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Health Plan News

Timely Health Plan News and Commentary

Health Plan News
Home Archives for Healthcare Policy and Law

Healthcare Policy and Law News

Health care in the United States is governed by an overlapping set of federal laws, state laws, agency rules and court decisions. The Affordable Care Act (ACA), the Medicare and Medicaid statutes, the Employee Retirement Income Security Act (ERISA) for employer plans, the No Surprises Act for out-of-network billing, and the Health Insurance Portability and Accountability Act (HIPAA) for privacy all shape what health plans may do and what patients can expect.

What We Cover

This section reports on legislation in Congress and state legislatures, rules issued by the U.S. Department of Health and Human Services (HHS) and the Centers for Medicare & Medicaid Services (CMS), state insurance department actions, enforcement by state attorneys general, and the lawsuits, settlements and court rulings that affect health plans, providers and patients. Medical malpractice litigation and patient safety cases are also covered here.

Policy changes ripple through the rest of the site. Marketplace and employer coverage rules appear in our Health Insurance Coverage reporting. Program rules for older adults and low-income households appear in Medicare and Medicaid and CHIP. Drug pricing and pharmacy benefit manager reform is covered in Prescription Drugs and Pharmacy, and price transparency and data privacy rules that affect technology vendors appear in Health Technology and AI.

Our reporting relies on primary sources wherever possible: the text of bills and regulations, agency announcements, and court filings. This content is news and general information, not legal advice.

The latest healthcare policy and law news appears below, newest first.

MagMutual Names Mike Beckett as Regional Vice President, Georgia

Posted on August 27, 2014 Written by Editor

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MagMutual Insurance Company, the Southeast’s policyholder-owned professional liability insurer, has promoted Mike Beckett to regional vice president for Georgia. He will lead the sales and policyholder services across the company’s first and largest market.

Beckett’s appointment extends a strategic focus by MagMutual on regional leadership that:

— improves service at the local level;
— closely aligns sales, claims, underwriting and risk management/patient safety; and
— allows greater presence and influence within Georgia’s medical, legislative legal and regulatory communities.

Beckett brings more than 20 years of malpractice insurance experience to his new role, having worked at MagMutual since 2002 as an account executive, director of retention for Georgia and vice president of premium accounts.

He holds a master’s of business administration from DeVry University and an undergraduate degree from College of Charleston.

Related Coverage

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For more reporting on this topic, see our Healthcare Policy and Law news hub.

Filed Under: Healthcare Policy and Law

Laugh Your Way to Good Health!

Posted on March 7, 2013 Written by Editor

Human beings have been laughing for as long as we have been human. In fact, recent evidence suggests that apes and other animals also laugh in their own way. And although humor is experienced across all ages and cultures, scientists are still not in agreement about the root causes of humor and laughter. For more in-depth information about humor and laughter, please check this out: http://en.wikipedia.org/wiki/Humor_(positive_psychology)#Humor_and_Health

laughing

Health and laughter
There is widespread agreement among scientists that humor in general, and laughter in particular, are very good for us. In fact, laughter provides a number of very powerful physical and emotional health benefits. [Read more…]

Filed Under: Healthcare Policy and Law

ESKADENIA Solutions Successfully Automates Emirates Group Medical Insurance Operations

Posted on January 29, 2013 Written by Editor

The Emirates Group comprised of Emirates airline and dnata, which has multiple business interests in the aviation, travel, tourism and leisure industries (Emirates Group), chose ESKADENIA Software Medical Insurance System to run the medical operations of more than 104,000 employees with their dependants.

The Emirates Group chose ESKADENIA’s Medical System due to its powerful claims audit tools and efficient network management that gives full details on the medical providers (Doctors, Pharmacies, Laboratories, and Hospitals) used by the Group.

ESKADENIA’s Medical Insurance System was customized to handle its employees’ medical claims in the most efficient and comprehensive manner. The Emirates employees can access their medical profile online and monitor their benefits, limits and utilization. In addition, they can submit claims directly from the web, request for medical approvals, and appeal for rejected claims.

It is worth to mention that ESKADENIA Medical Insurance system works for both individuals and groups, also it complies with governmental regulations, which makes it an easy to- use tool for the recording and manipulation of insurance policy production, medical networks, claims, policy renewals, and reinsurance operations.

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  • Medical Tourism Association® Joins Forces to Launch Asia-Pacific 2015 Global Healthcare Congress

For more reporting on this topic, see our Healthcare Policy and Law news hub.

Filed Under: Healthcare Policy and Law

Cooper Health System Pays $12.6 Million To Resolve False Claims Lawsuit

Posted on January 24, 2013 Written by Editor

A federal lawsuit filed by prominent Delaware Valley cardiologist Nicholas L. DePace, M.D., sparked a multi-year investigation by the United States Department of Justice and the New Jersey Attorney General’s Office that has resulted in New-Jersey based Cooper Health System, and Cooper University Hospital paying $12,600,000 to settle Medicare and Medicaid fraud allegations.

According to Dr. DePace’s Complaint, since 2004, Cooper funneled illegal kickbacks to referring physicians through an advisory board known as the Cooper Heart Institute Advisory Board (“CHIAB”). Cooper established the CHIAB in 2004, with the stated purpose of utilizing prominent New Jersey physicians to advise the Cooper Heart Institute regarding innovative technologies, new management strategies, community needs, and appropriate educational and research initiatives.

In reality, the CHIAB was a sham, in which Cooper paid physicians with high-volume medical practices upwards of $18,500 each to do little more than watch four lectures per year hosted at an elegant banquet facility. These lectures consisted mostly of marketing presentation on cardiac care at Cooper. Additional lectures included generic subjects that were irrelevant to the stated mission of the CHIAB, including a 2008 lecture entitled: “The Healthcare Plans of the Two Presidential Candidates.”

In the spring of 2007, Cooper invited Dr. DePace to join the CHIAB. After attending his first CHIAB lecture, Dr. DePace quickly realized that the CHIAB was a thinly-veiled kickback scheme. Dr. DePace observed that the other CHIAB members were family physicians with high-volume practices. These physicians were all in the position to direct millions of dollars in patient care to Cooper.

Dr. DePace also observed that the CHIAB physicians were paid $18,500 for doing nothing more than sitting and listening to marketing presentations and lectures on irrelevant topics. The physicians did not discuss the lecture topics, and were not required to perform any additional work in exchange for the payments from Cooper.

In exchange for Cooper’s kickback payments, CHIAB physicians referred their patients to the Cooper Heart Institute for expensive in-patient and out-patient cardiac services. At least one CHIAB member admitted to Dr. DePace that, when making referrals, he knew that Cooper, through the CHIAB, “butters his bread.”

The settlement with the United States, and the State of New Jersey, announced today, will require Cooper to pay the United States $10,000,000 and the State of New Jersey $2,600,000. The settlement is one of the largest against a hospital for operating a kickback scheme, and is one of the largest recoveries for the State of New Jersey under its recently passed state False Claims Act. Cooper denies that it is liable for violating federal or state laws.

Related Coverage

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For more reporting on this topic, see our Hospitals and Health Systems news hub.

Filed Under: Healthcare Policy and Law, Hospitals and Health Systems

ACLJ Files 4th Direct Challenge To HHS Mandate

Posted on January 24, 2013 Written by Editor

The American Center for Law and Justice (ACLJ), a pro-life legal organization that focuses on constitutional law, today filed its fourth direct challenge to the mandate of the Department of Health and Human Services (HHS) on the basis that the mandate violates the religious beliefs of business owners. The lawsuit was filed today in the U.S. District Court for the District of Columbia and contends that the HHS mandate violates constitutional and statutory rights by requiring two Ohio companies and their owners to purchase health insurance for employees that include coverage for contraception, sterilization and abortion-inducing drugs.

The lawsuit, posted here: http://c0391070.cdn2.cloudfiles.rackspacecloud.com/pdf/complaint-declaratory-injunctive-relief-freshway-v-hhs.pdf, argues that the HHS mandate violates the First Amendment, the Religious Freedom Restoration Act, and the Administrative Procedure Act.

The lawsuit contends the HHS mandate forces the owners to “violate their religious beliefs and moral values” or face crippling fines and penalties. For the two companies combined, the fines and penalties would total nearly $40,000 a day, amounting to $14.4 million annually, which the owners contend will be “ruinous” for their businesses.

Related Coverage

  • American College of Emergency Physicians, American College of Radiology, and American Society of Anesthesiologists File Lawsuit
  • Historic Settlement Reached Against Clark County School District for $9.95 Million

For more reporting on this topic, see our Healthcare Policy and Law news hub.

Filed Under: Healthcare Policy and Law

Majority Of U.S. Voters Think Legal System Increases Cost Of Health Care

Posted on May 29, 2012 Written by Editor

A new nationwide poll finds that heavy majorities of voters across party lines believe that the legal system is increasing health care costs. The survey also found that 66 percent of voters favor taking medical claims out of the current legal system and putting them into new health courts with expert judges. The poll was conducted for Common Good by Clarus Research Group.

Among the poll’s key findings are the following:

— A strong majority of voters––75 percent––believe “lawsuits and legal fees are a major cause of high medical insurance rates.” Eighty-nine percent of Republicans, 76 percent of independents and 62 percent of Democrats agree on this.

— Sixty-eight percent agree that “plenty of good doctors are leaving the practice of medicine because of the number of lawsuits and the cost of liability insurance.” Seventy-eight percent of Republicans, 64 percent of Democrats and 61 percent of independents agree. [Read more…]

Filed Under: Healthcare Policy and Law

Poll: Americans Overwhelmingly Support Strong Medical Device Safety Oversight

Posted on March 20, 2012 Written by Editor

A new Consumer Reports poll shows overwhelming public support for strong medical device safety oversight. The poll was released just as House and Senate Committees have issued draft legislation to reauthorize the statute governing medical devices and at a time when the FDA’s process for reviewing new implants has come under intense criticism.

The House Energy and Commerce Health Subcommittee’s draft bill would significantly weaken device safety oversight and should be rejected by Congress, according to Consumers Union, the policy and advocacy arm of Consumer Reports. While the Senate Health, Education, Labor and Pensions Committee’s draft bill provides some additional protections for patients once devices are on the market, it misses the opportunity to enact a clear process for preventing unsafe devices from being sold in the first place.

The medical device industry has been pushing Congress to scale back oversight of implants and other devices, which it claims is necessary to promote innovation and make it easier to get new devices approved. But according to the new Consumer Reports poll, 82 percent of Americans believe that preventing safety problems is more important than limiting safety testing in order to prevent delays and encourage innovation. [Read more…]

Filed Under: Healthcare Policy and Law, Prescription Drugs and Pharmacy

Maryland’s Cancer Care Community, Patient Advocates Urge State Legislature to Create Parity in Coverage for Preferred Cancer Drugs

Posted on February 5, 2012 Written by Editor

Citing the significant quality of life benefits that oral chemotherapy drugs can provide over intravenously (IV) administered chemotherapy, Maryland’s cancer community, patient advocacy representatives and patients themselves called on the state legislature this week to pass key legislation that would ensure Maryland’s cancer patients are able to access their prescribed chemotherapy regimen of choice.

IV chemotherapy can lead to side effects including pain, hair loss, nausea, vomiting, and anemia, and can lead to added costs and logistical issues as patients must travel to cancer care facilities for treatment. Although oral chemotherapy drugs taken at home often result in fewer side effects, many health insurance plans’ coverage of orally administered chemotherapy is prohibitive due to higher copays, expensive deductibles or restrictive coverage limits.

The Kathleen A. Mathias Chemotherapy Parity Act of 2012 (Senate Bill 179) would prohibit insurers, nonprofit health service plans, and health maintenance organizations (HMOs) from covering orally administered cancer chemotherapy on terms that are less favorable than coverage for IV administered cancer chemotherapy. The bill is named in honor of the late Kathy Mathias, wife of Sen. Jim Mathias (D-38), who lost her 14-year battle with cancer last August. The legislation currently has 26 cosponsors in the Senate and will be heard before the Maryland House Health and Government Operations Committee on February 9.

In testimony this week before the Maryland Senate Finance Committee, Larry L. Lanier, NPAF Vice President of State Government Affairs, noted that parity in chemotherapy drug coverage remains an important issue for patients, with many contacting PAF on a regular basis in need of assistance to cover the cost of oral chemotherapy medications. Additional testimony was provided by representatives from The Maryland/District of Columbia Society of Clinical Oncology, the Maryland State Medical Society (MedChi), the Leukemia and Lymphoma Society (LLS), additional Maryland-based advocates, and patients who would benefit from the passage of this legislation.

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Filed Under: Healthcare Policy and Law, Public Health and Research

Organ Donation Association Supports Living Organ Donation

Posted on February 5, 2012 Written by Editor

Currently, there are more than 112,000 patients on the national organ transplant waiting list. These candidates often endure difficult yet necessary life-sustaining treatments while waiting for potential organ matches. Nineteen people die every day while waiting, and those that are eventually transplanted can endure wait times that can extend anywhere from 5-9 years.

The need for life-saving organ transplants was recently highlighted when New England Patriots quarterback Tom Brady shared his friend and long-time coach is in need of a kidney transplant. The Association of Organ Procurement Organizations applauds Brady for the attention he has brought to living donation specifically and to all organ and tissue donation in general.

Organ procurement organizations (OPOs) are the national stewards of the precious gift of life. During 2011 the 58 federally designated OPOs helped more than 8,000 deceased donors and their families give the gift of organ donation. Several OPOs, in collaboration with their local transplant centers also have programs that support and facilitate living organ donation.

The most effective way to save lives through organ donation is by registering your personal decision through your state designated donor registry. Each state has a Uniform Anatomical Gift law that protects and facilitates deceased donation. For more information about donation or how to become a designated donor in your state, please visit Donate Life America at http://donatelife.net.

Related Coverage

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For more reporting on this topic, see our Healthcare Policy and Law news hub.

Filed Under: Healthcare Policy and Law

Virginia Governor Signs Autism Insurance Reform Into Law

Posted on May 7, 2011 Written by Editor

This afternoon, the Virginia Autism Project joined families and communities in Virginia in applauding Governor Robert McDonnell in signing Home Bill 2467 and Senate Bill 1062, which will become law effective January 1, 2012.

This new law demands insurance companies to offer evidence-based, medically necessary autism therapies for children ages 2 thru 6 with a $35,000 annual cap. Sponsored by Senator Janet Howell (Fairfax-D) and Delegates Tim Hugo (Fairfax-R), Tom Rust (Fairfax/Loudoun-R), and Tag Greason (Loudoun-R), this reform passed the General Assembly with overwhelming support last month following 11 years of failed attempts.

[Read more…]

Filed Under: Healthcare Policy and Law

FTC Settles with NBTY, NatureSmart, and Rexall Sundown Over Deceptive Claims about DHA and Brain and Eye Development

Posted on March 29, 2011 Written by Editor

The Federal Trade Commission has finalized an Order that settles charges that NBTY, NatureSmart, and Rexall Sundown made false and unsupported claims that their Disney and Marvel Heroes line of children’s multivitamins contained a significant amount of DHA (docosahexaenoic acid, an Omega-3 fatty acid) and promoted healthy brain and eye development in children. As part of the settlement in this case, which was first announced in December 2010, NBTY, Inc. and two subsidiaries, NatureSmart LLC and Rexall Sundown, Inc have agreed to pay $2.1 million to provide refunds to consumers who purchased these multivitamins.

Part of the Order is listed below:

The Federal Trade Commission having initiated an investigation of certain acts and practices of the respondents named in the caption hereof, and the respondents having been furnished thereafter with a copy of a draft of complaint which the Bureau of Consumer Protection proposed to present to the Commission for its consideration and which, if issued by the Commission, would charge the respondents with violations of the Federal Trade Commission Act; and The respondents and counsel for the Commission having thereafter executed an agreement containing a consent order, an admission by the respondents of all the jurisdictional facts set forth in the aforesaid draft complaint, a statement that the signing of the agreement is for settlement purposes only and does not constitute an admission by the respondents that the law has been violated as alleged in such complaint, or that any of the facts as alleged in such complaint, other than jurisdictional facts, are true, and waivers and other provisions as required by the Commission’s Rules; and

The Commission having thereafter considered the matter and having determined that it had reason to believe that the respondents have violated the Act, and that complaint should issue stating its charges in that respect, and having thereupon accepted the executed consent agreement and placed such agreement on the public record for a period of thirty (30) days for the receipt and consideration of public comments, and having duly considered the comments received from interested persons, now in further conformity with the procedure described in Commission Rule 2.34, 16 C.F.R. § 2.34, the Commission hereby issues its complaint, makes the following jurisdictional findings, and issues the following order:

1. Respondent NBTY, Inc. is a Delaware corporation with its principal place of business

located at 2100 Smithtown Ave., Ronkonkoma, New York 11779.

2. Respondent NatureSmart LLC is a Colorado limited liability company with its principal place of business at 2100 Smithtown Ave., Ronkonkoma, New York 11779.

3. Respondent Rexall Sundown, Inc., also doing business as Sundown, Inc., is a Florida corporation with its principal place of business at 2100 Smithtown Ave., Ronkonkoma, New York 11779.

4. The Federal Trade Commission has jurisdiction of the subject matter of this proceeding and of the respondents and this proceeding is in the public interest. [Read more…]

Filed Under: Healthcare Policy and Law

Civil Penalties to be Imposed on Herbal Products Company Daniel Chapter One

Posted on March 28, 2011 Written by Editor

The U.S. Department of Justice, via a request by the FTC, has asked a federal district court to impose civil penalties upon an herbal products company named “Daniel Chapter One (DCO)” and its principal, James Feijo, for allegedly violating an FTC Order.

The civil penalty action also seeks a preliminary injunction to stop DCO and Feijo from continuing to make deceptive claims on the company’s daily radio show and website about the supposed cancer-fighting properties of its supplements, and to require DCO and Feijo to send a notice to purchasers explaining the FTC’s findings that the advertisements were unsubstantiated, as required by the FTC Order.

Daniel Chapter One and Feijo deceptively advertised that four dietary supplements – BioShark, 7 Herb Formula, GDU, and BioMixx – inhibit tumor formation or growth, eliminate tumors, treat or cure cancer, or heal the effects of radiation or chemotherapy. An administrative trial took place in April 2009, and the Administrative Law Judge found that the defendants were making deceptive claims. The Commission upheld the ALJ’s initial decision in December 2009.

As part of the FTC Order issued in December 2009, Daniel Chapter One and Feijo were required to stop making the deceptive claims, and to send a notice to purchasers explaining the FTC’s findings that advertising claims for the supplements were unsubstantiated, and that consumers should consult with health care providers before using any herbal product, to ensure that all aspects of their medical treatment work together.

Related Coverage

  • FTC Settles with NBTY, NatureSmart, and Rexall Sundown Over Deceptive Claims about DHA and Brain and Eye Development

For more reporting on this topic, see our Healthcare Policy and Law news hub.

Filed Under: Healthcare Policy and Law

Topamax Lawsuits on the Rise

Posted on March 24, 2011 Written by Editor

Topamax (topiramate), when taken by pregnant women, greatly increases the risk that their babies will develop birth defects, like cleft lips and cleft palates, the U.S. Food and Drug Administration warned recently. Alternative medications have lower risks of causing birth defects, and women treated with Topamax during pregnancy whose children were born with birth defects are increasingly filing suit to be compensated. Johnson Law Group is evaluating and accepting Topamax cases now.

“More than 4.3 million patients filled Topamax prescriptions in the U.S. in the last four years,” said Attorney Nick Johnson, founder of Johnson Law Group. “That includes a significant number of women who may never have known how dangerous Topamax could be for their developing infants. Those women and children deserve justice.”

The FDA has said, “…topiramate is being placed in Pregnancy Category D. Pregnancy Category D means there is positive evidence of human fetal risk … an increased risk for oral clefts … based on human data.” Previously the drug was listed as a Category C drug, which recognizes that animal studies “suggested potential fetal risk.”

Topamax (topiramate) is an anticonvulsant medication used, sometimes in conjunction with other medications, to treat epilepsy patients with certain types of seizures, and sometimes to prevent migraine headaches.

If you would like to file a complaint, or simply need more information about the birth defects caused by Topamax, call 1-800-217-9891 or visit: http://pharmaceuticals.johnsonlawgroup.com/topamax-and-birth-defects.

Johnson Law Group is comprised of experienced personal injury attorneys. The firm offers legal and medical professional investigative skills, expert witnesses, cutting-edge technology, and state-of-the-art techniques for maximum recovery. Nick Johnson leads the Johnson Law Group. He graduated from Duke University and the University of Houston Law Center. Mr. Johnson practices in all areas of personal injury law, with a primary focus on pharmaceutical and asbestos related lung cancer cases.

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Filed Under: Healthcare Policy and Law, Prescription Drugs and Pharmacy

FONAR UPRIGHT MRI Customer Wins Jury Decision in Federal Court for Antitrust Lawsuit Versus CareCore National

Posted on December 13, 2010 Written by Editor

SOURCE: FONAR Corporation

MELVILLE, NY–(Marketwire – December 13, 2010) – FONAR Corporation (NASDAQ: FONR), The Inventor of MR Scanning™, announced today that a provider of outpatient diagnostic services (a FONAR customer) and several Stand-Up MRI diagnostic imaging professional corporations (PCs) received a jury verdict in their favor in an anti-trust lawsuit against CareCore National, LLC, a radiology benefits management (RBM) company (www.carecorenational.com).

This antitrust lawsuit involved CareCore National’s exclusion of the plaintiffs, all of them providers of MRI services using Stand-Up MRI scanners (FONAR UPRIGHT® Multi-Position™ MRIs), from utilization by its member subscribers. CareCore Radiology, a division of CareCore National, covers more than 30 million member subscribers in all 50 states. The diagnostic service provider and the PCs were represented by Constantine Cannon LLP, New York, NY, (www.constantinecannon.com). 

After more than a two-week trial, the verdict was reached November 30, 2010 in the U.S. District Court for the Eastern District of New York. The case is Stand-Up MRI v. CareCore National, E.D.N.Y. Case No: 08 Civ. 2954 (LDW) (ETB). The eight members of the jury were unanimous in their decision and awarded over $11 million in damages to the diagnostic service provider and the PCs in the case, which are to be trebled by law. The total judgment with costs and attorney fees is expected to be close to $40 million.

In a press release, (http://www.prnewswire.com/news-releases/constantine-cannon-attorneys-win-important-healthcare-antitrust-jury-trial-against-carecore-national-llc-111128319.html) lead Constantine Cannon trial attorney Matthew Cantor said: “This verdict is not just important for my clients, but for patients everywhere. The evidence in this case showed that even CareCore considered the Upright MRI to be medically necessary and that, nonetheless, CareCore and its owners denied patients the ability to benefit from these important diagnostic procedures. The actions of benefits managers (RBMs) that are owned and controlled by physicians, like CareCore, must be scrutinized to ensure that patient welfare is not compromised. Constantine Cannon expects that the defendants will attempt to overturn the jury award either in post-trial motion practice or on appeal. If that occurs, Constantine Cannon will vigorously defend the decision of the jury.”

“The jury found that CareCore, in league with New York-area radiologists and radiology practices that owned and/or governed CareCore, conspired to unreasonably restrain trade in the market for commercially-insured outpatient radiology procedures. The jury also found that these restraints harmed the plaintiffs — several New York radiology practices and their medical management company — that offer unique and medically necessary Upright MRI services. The Upright MRI is the only MRI that can scan patients in the weight-bearing positions that patients actually feel their pain. By doing so, Upright MRIs diagnose patient ailments, including those related to the spine, that no other MRI can,” said Cantor.

Raymond Damadian, president and founder of FONAR said, “We are pleased that the Federal Court and Jury understands the medical necessity of the FONAR UPRIGHT® Multi-Position™ MRI aka STAND-UP® MRI. This is important for FONAR, its customers, future customers and particularly the patients who need the UPRIGHT® MRI so they can be correctly diagnosed and not be given the wrong treatment which often involves surgery. We expect this to help those patients across our nation who have been previously denied these critical examinations by the RBMs.”

“FONAR’s UPRIGHT® MR technology is vital to patient needs nationwide,” said Dr. Damadian. “Back pain is the second most common reason for visiting the doctor’s office after the common cold. Close to one million spine surgeries are performed each year, but the outcomes are not good with a failure rate that varies from 10% to 40% depending on the reported study (1). Alf Nachemson, MD refers to the saddest group of these patients, those who have undergone 4, 5, or 6 spine surgeries as “multiply operated surgical cripples” (2). The surgical failure is commonly the result of operating on the wrong spinal segment (i.e. not the one responsible for the patient’s pain). This occurs because the origin of the pain is often attributed to the wrong degenerative change in the spine when the patient is imaged on a recumbent-only MRI. Degenerative changes in the adult spine are frequently multiple in number. The suspected pain generating anatomy is conventionally identified from recumbent (conventional) MRI images while the patient’s pain often occurs only when the patient is upright and when the pathology generating it is visible only when the patient is upright and fully weight-loaded.”

Dr. Damadian continued, “The FONAR UPRIGHT® Multi-Position™ MRI enables the patient to place himself in the position that generates his pain so that an MRI picture can be taken in the same position that generated the patient’s pain. Correctly identifying the pain generating pathology markedly improves patient surgical outcomes. In addition, it enables the surgeon to see ALL the pathology he has to address, not just the single position non-weight-bearing image provided by the conventional MRI. This enables the surgeon to see the full extent to which the disk herniation of his patient increases when he/she flexes or extends, or the extent to which the patient’s vertebra is sliding back and forth with body position and generating pain. Approximately 1 million spine surgeries are performed in the U.S. each year and technology to improve the surgical outcomes for these patients is a serious need.”

“In addition, there are a wide range of other needs that patients have for FONAR’s UPRIGHT® Multi-Position™ MR imaging technology,” said Dr. Damadian. “Patients who have been hospitalized, for example, with congestive heart failure, cannot lie down. In the absence of UPRIGHT ® MRI these patients are unable to receive MRI examinations when they are needed.”

“Patients with scoliosis, which most commonly arises for the first time in young adolescent girls, have been reported by the National Cancer Institute (3) to experience a 70% higher incidence of breast cancer as adults than the non-scoliotic population. The increased incidence is attributed to the multiple annual chest x-rays (2-3 times per year) needed to monitor the child’s scoliosis until adulthood in order to assure satisfactory treatment.” Dr. Damadian added, “the FONAR UPRIGHT® MRI provides the same necessary vertebral angle (“Cobb angle”) measurements as the x-ray (plus the needed measurements of vertebra rotation not supplied by x-ray), thereby avoiding the annual radiations of the x-ray procedure and eliminating the danger of subsequent adult breast cancer.”

“Women patients, for example, as a result of the inherent trauma of childbirth to their pelvic floor anatomy, will commonly suffer the consequences of PFD (pelvic floor dystrophy) later in life. The symptoms of PFD are cystic prolapse (“falling urinary bladder”) and its chronic cystitis symptoms of urinary frequency, burning on urination, fever, and if unaddressed, chronic kidney inflammation (pyclonephritis). The patient must be upright to see it. It commonly returns to its normal position when the patient is recumbent and therefore is not diagnosed by the patient’s physician who examines her in the recumbent position. It affects 10 million women. The UPRIGHT® MRI readily visualizes the fallen bladder when these patients are upright, so that the surgeon has full image visualization of the anatomy that has to be repaired.

“Another serious present need for the FONAR UPRIGHT® Multi-Position™ MRI is the rising body of patients who are sustaining dislocations of the cervical spine from automobile collision whiplash injuries of the head and neck. The UPRIGHT® MRI is needed to assess the extent to which the brain has been dislocated [descent of the tonsils of the cerebellum] into the opening in the bottom of the skull (foramen magnum). This critical assessment of the extent of brain herniation into the opening at the base of the skull (cerebellar tonsil ectopia, or CTE) can only be determined with the patient in the upright position so that the surgical repair of this herniation and the patient’s “drop attacks” can be eliminated. (4)”

(1) The Failed Spine, M. Szpalski and R. Gunzburg, eds., Lippincott Williams & Wilkins, 2005, p. 123.
(2) Alf L. Nachemson, MD, “The Lumbar Spine An Orthopaedic Challenge”, Spine, Vol. 1, Number 1, March 1976, p. 65.
(3) National Cancer Institute, “Scientists Find Link Between Pre-1970’s Diagnostic X-rays for Scoliosis and Breast Cancer Mortality,” www.cancer.gov, 8/15/2000. “Breast Cancer Mortality  After Diagnostic Radiography: Findings from the U.S. Scoliosis Cohort Study”, Michele Morin Doody, et al., Spine, Aug. 15, 2000, Vol. 25, No. 16.
(4) Michael D. Freeman, et al., Brain Injury, July 2010:24(7-8):988-994.

About Constantine Cannon LLP

Constantine Cannon LLP represented the plaintiffs in the case. They have deep expertise in practice areas that include antitrust and complex commercial litigation, government relations, employment matters, securities and e-discovery. With offices in New York, NY and Washington, DC, the firm’s antitrust practice is among the largest in the nation, with more than 30 attorneys representing both plaintiffs and defendants in complex antitrust litigation.

For investor and other information visit: www.fonar.com.

UPRIGHT® and STAND-UP® are registered trademarks and The Inventor of MR Scanning™, Full Range of Motion™, pMRI™, Dynamic™, Multi-Position™, True Flow™, The Proof is in the Picture™, Spondylography™ Spondylometry™ and Upright Radiology™ are trademarks of FONAR Corporation.

This release may include forward-looking statements from the company that may or may not materialize. Additional information on factors that could potentially affect the company’s financial results may be found in the company’s filings with the Securities and Exchange Commission.

Filed Under: Healthcare Policy and Law

Mitchell International Closes Purchase of Ingenix Property & Casualty Medical Bill Review Business

Posted on December 7, 2010 Written by Editor

SOURCE: Mitchell International

Smooth Leadership and Technology Transition Ensures Successful Integration of Customer Medical Bill Review Operations Into SmartAdvisorTM Medical Bill Review Platform

SAN DIEGO, CA–(Marketwire – December 7, 2010) – Mitchell International, Inc., a leading provider of information, workflow and performance management solutions to the Property & Casualty (P&C) claims and Collision Repair industries, today announced the successful close of its purchase of Ingenix’s P&C medical bill review (MBR) business. The purchase places Mitchell Workers’ Compensation Solutions (WCS) business and its SmartAdvisor™ medical bill review platform in a market leadership position, enabling the company to deliver to the insurance and managed care related industries advanced technology solutions with a proven track record of streamlining medical claims operations and improving cost containment.

“Since the intent to purchase the Ingenix MBR business was announced this October 20, Mitchell has experienced broad market acceptance and customer buy-in, the result of a carefully planned business and technology transition strategy that is being deployed within the context of Mitchell’s stable position and long-term experience in the P&C marketplace,” said Nina Smith-Garmon, senior vice president and general manager of the Mitchell Workers’ Compensation Solutions Division.

Smith-Garmon added, “The positive feedback we have received at the recent National Workers’ Compensation and Disability Conference® & Expo indicates that Ingenix P&C MBR customers anticipate a smooth, successful transition to Mitchell and the SmartAdvisor medical bill review technology platform. We will continue to enhance our solution for all our customers by adding to our already-extensive Preferred Provider Organization (PPO) networks and compliance expertise via strategic partnerships and acquisitions.”

Mitchell SmartAdvisor is a comprehensive bill review solution for workers’ compensation that leads the industry in its unique combination of performance software, client services, and best-in-class partnerships. Available through licensed or software-as-a service model, SmartAdvisor’s unique capabilities include customizable workflow modeling, Capstone® business decision rules engine, data analytics and reporting tools, Claims Examiner Portal for fast, secured, real-time access to bill data, and a proven technology platform that delivers on average 50-70% straight-through processing for improved efficiencies and lower costs. Visit www.mitchell.com/smartadvisor for more information or contact Mitchell Workers’ Compensation Solutions directly at 1-800-421-6705 to schedule a demo of the SmartAdvisor bill review system.

About Mitchell International, Inc.
Mitchell International (www.mitchell.com) is a leading provider of information and workflow solutions to the Property & Casualty claims and Automotive Collision Repair industries. The company’s comprehensive solution portfolio streamlines the entire auto physical damage, bodily injury and workers’ compensation claims processes. Mitchell enables millions of electronic transactions between more than 30,000 business partners each month to enhance partner productivity, profitability, and customer satisfaction.

About Mitchell Workers’ Compensation Solutions Division
Mitchell Workers’ Compensation Solutions (WCS), a division of Mitchell International, is a leading provider of workers’ compensation cost containment technologies and services. Insurance payers and other clients rely on Mitchell WCS’s best-of-breed medical bill review platform, the SmartAdvisor Software Suite, to improve their medical cost savings results. For more information, please visit www.mitchell.com/smartadvisor.

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Filed Under: Health Technology and AI, Healthcare Policy and Law

ForceLogix Technologies Inc. Announces Filing of Interim Financial Statements and Management’s Discussion and Analysis

Posted on November 29, 2010 Written by Editor

SOURCE: ForceLogixTechnologies Inc.

CHICAGO, IL–(Marketwire – November 29, 2010) – ForceLogix Technologies Inc. (TSX-V: FLT) is pleased to announce that it filed its interim financial statements and Management’s Discussion and Analysis today for the quarter ended September 30, 2010. The financial statements are available for review on SEDAR, www.sedar.com.

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

For further information please contact:
Nick Blair
847 327 0306
Email Contact

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Filed Under: Healthcare Policy and Law

Prolitec Names Bhandari Director of Business Development

Posted on October 26, 2010 Written by Editor

SOURCE: Prolitec

MILWAUKEE, WI–(Marketwire – October 26, 2010) –  Prolitec Inc., a leading developer of air treatment and air care technologies, today announced the appointment of Suresh Bhandari, 45, as Director of Business Development.

 In his new position, Mr. Bhandari, who is based in the Washington, D.C. area, will be responsible for managing the company’s government sales effort nationwide.

Bhandari comes to Prolitec from First American Corporation, a Fortune 500 company and the leader in providing nationwide property information and analytics in support of the financial and real estate sectors, where he served as Director, Federal Solutions since 2007. In that capacity, he was responsible for managing sales, marketing and GSA/GWAC functions for the company’s federal business unit. 

 Prior to that, Bhandari established the Federal Practice for Global Consultants, a $200 million IT solutions and staffing company based in Herndon, Va. As General Manager, he directed all phases of the Federal Practice’s strategy, marketing, sales, operations, and client relationships.

Earlier in his career, Bhandari worked in sales and marketing at several software and information systems companies. He began his career in 1996 as a regional sales manager for Upspring Software, Inc., Lexington, Mass., and went on to serve as vice president of sales and marketing at Rjay Consultants, Inc., Sterling, Va.; director of marketing and strategic alliances at Invertix Corporation, Alexandria, Va.; and vice president, strategic relations, Artech Information Systems, McLean, Va., before joining Global Consultants in 2004.

Mr. Bhandari, a resident of Oakton, Va., earned a Master of Science degree in computer science from Arizona State University, Tempe, Ariz.; a Bachelor of Engineering in computer engineering and science from Bangalore University, Bangalore; and, concurrently, a Diploma in Commerce, with emphasis on marketing & sales, commerce, accounting and mercantile law from Davars College of Commerce, Bangalore. 

About Prolitec
Prolitec (www.prolitec.com) develops and deploys air-treatment and air care technologies for healthcare facilities, hotels, casinos, and other institutional and commercial facilities in the U.S. and 46 countries around the world. The company’s Aerobiology and Infection Control division is engaged in the development and deployment of airborne and surface antimicrobial systems to inhibit disease transmission. 

Filed Under: Healthcare Policy and Law

Pharos Innovations CEO Named to Head Government Affairs Committee of the Care Continuum Alliance

Posted on October 21, 2010 Written by Editor

SOURCE: Pharos Innovations

NORTHFIELD, IL–(Marketwire – October 21, 2010) –  Randall E. Williams, MD, CEO and founder of Pharos Innovations, has been elected to chair the Government Affairs Committee of the Care Continuum Alliance, an organization focused on strategies to improve healthcare quality and outcomes and reduce preventable costs. As chair of the Government Affairs Committee, Dr. Williams will provide leadership and oversight for the committee’s work including the development of position statements on emerging public policy issues, as well as monitoring healthcare policy to provide Care Continuum Alliance members with valuable information and research on key legislative and regulatory issues. Dr. Williams is also a member of the Alliance’s Executive Committee, which is comprised of healthcare leaders from health plans, academia, wellness organizations and other health management stakeholders.

“I am very honored to have been selected to chair The Care Continuum Alliance’s Government Affairs Committee. I hope to draw from my past work with key Congressional committees, HHS and CMS as we work to accomplish the ‘triple aim’ of improving healthcare quality, reducing healthcare costs and improving the health of populations and sustainability of our healthcare system,” said Williams. “The Care Continuum Alliance is a thought-leadership organization with a wealth of collective experience moving in the right direction toward these aims, and I am excited to be part of this movement.”

Under Dr. Williams’ leadership, Pharos Innovations developed Tel-Assurance®, a device-free, cost effective, remote patient monitoring platform that does not require special equipment. Tel-Assurance has helped Medicare, Medicaid and commercial patients and their physicians achieve break-through levels of clinical and financial performance improvement, including several successful CMS demonstrations.

“Dr. Williams brings exceptional credentials and experience to our Government Affairs Committee,” Care Continuum Alliance President and CEO Tracey Moorhead said. “His leadership will be invaluable as healthcare reform moves through the regulatory process.”

About the Care Continuum Alliance
The Care Continuum Alliance convenes all stakeholders providing services along the continuum of care for population health improvement, including health and wellness promotion, chronic care management and care coordination. Through advocacy, research and promotion of best practices, the Care Continuum Alliance advances population-based strategies to improve care quality and outcomes and reduce preventable costs for individuals with and at risk of chronic conditions. The Care Continuum Alliance represents more than 200 corporate and individual stakeholders, including wellness and care management organizations, pharmaceutical manufacturers and benefits managers, health information technology and biotechnology innovators, employers, hospitals, physicians, nurses and other health care professionals, and researchers and academics. Learn more at http://www.carecontinuum.org.

About Pharos Innovations
Pharos Innovations is actively involved in transforming the U.S. healthcare delivery system. Pharos offers IVR and Web-based behavior change services and tools that enable payers and providers to cost-effectively and efficiently manage their chronic care population.

Pharos’ main offering, Tel-Assurance, engages, motivates and drives improved self-care. Through Tel-Assurance, participants self-report their health status daily through the phone or Web. This unique approach actively engages individuals with chronic conditions in their healthcare and provides care managers/nurses with real-time information to intervene before symptoms escalate. Tel-Assurance has been proven an effective way to reduce avoidable, all-cause hospital admissions and readmissions and reduce overall healthcare costs among diverse populations.

The Pharos’ solution is strongly validated to show measured clinical improvement and financial impact, is the recipient of the prestigious American Heart Association National Outcomes award and was selected for the first ever National Institutes of Health (NIH) sponsored evaluation of remote monitoring interventions. For more information visit http://www.pharosinnovations.com or join in on the discussion at our blog, http://www.thecollaborativeforum.com.

Contact:
Shawn-Laree De St. Aubin
312-725-3740
Email Contact

Bonni L. Kaplan
Pharos Innovations
847-790-7649
Email Contact

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Filed Under: Healthcare Policy and Law, Medicare

WesternU Receives More Than $1.3 Million in Federal Grants

Posted on October 19, 2010 Written by Editor

SOURCE: Western University of Health Sciences

POMONA, CA–(Marketwire – October 19, 2010) – Western University of Health Sciences programs received more than $1.3 million in federal funding to enhance learning and bring critically-needed care to vulnerable populations.

The Department of Physician Assistant Education, part of the College of Allied Health Professions, received about $100,000 in Health Resources and Services Administration grant funding to buy 10 Student Auscultation Manikins.

The College of Dental Medicine (CDM) received about $180,000 in HRSA grant funding for Project TEACH (Training Equipment for Access and Community Health). The money will be used to provide mobile dental care to rural and underserved populations.

The College of Graduate Nursing (CGN) received about $1.05 million for students in the Family Nurse Practitioner (FNP) master’s program. The money will cover full tuition and educational expenses, as much as $22,000 per year, for six full-time students per year who, upon graduation, are planning to work with vulnerable populations in the delivery of Primary Care to patients in medically underserved areas. These underserved areas include those with “financial, racial, linguistic and cultural barriers to health care services and (to varying extents) need for services,” according to the National Health Policy Forum.

This grant expands access to primary care by allowing part-time FNP students to become full-time students so they can finish the program quicker and begin making a difference in the community.

The scholarships will also benefit new incoming FNP students who were accepted as part of CGN’s expansion. The FNP program averages 25 to 35 students per class. This year the program accepted 47 new students.

CDM is partnering with the Victor Valley Dental Center in Victorville to furnish the center’s mobile dental van with two fully-equipped dental chairs, said Timothy Martinez, DMD, CDM Associate Dean for Community Partnerships and Access to Care. CDM students will travel with the mobile van to schools in the Victorville area to treat students.

The grant funding also paid for three portable digital radiographic units, three portable sterilization units and two complete hand piece set ups. These portable units will help the college address multiple needs, such as providing dental care to students in the El Monte and Pomona unified school districts.

CDM will also provide perinatal dental education and prevention services for the California Department of Health’s Black Infant Health (BIH) program, which provides health education, health promotion, social support and service coordination to pregnant women and their children.

The Department of Physician Assistant Education will use about $100,000 in federal funding to improve student education and testing by purchasing 10 torso mannequins that simulate heart, lung and abdomen sounds.

Students could listen to each other’s heartbeat and breathing, but they would typically not be exposed to the broad range of abnormal sounds that they need to learn, said Tina Boykin-Mowrey, MPH, MS, PA-C, PA Department Clinical Education Coordinator.

“This will expand our training capabilities,” she said.

Contact:
Rodney Tanaka
Office: (909) 469-5402
E-mail: [email protected]

Filed Under: Healthcare Policy and Law

CytoSorbents Corporation Selected to Present at the 2010 AdvaMed MedTech Conference

Posted on October 11, 2010 Written by Editor

SOURCE: CytoSorbents Corporation

MONMOUTH JUNCTION, NJ–(Marketwire – October 11, 2010) –  CytoSorbents Corporation (OTCBB: CTSO), a critical care focused company using blood purification to treat life-threatening illnesses, was chosen to present at the AdvaMed 2010 MedTech Conference at the Walter E. Washington Convention Center in Washington, D.C. next week. Dr. Phillip Chan, Chief Executive Officer, will speak Wednesday, October 20, 2010 at 10:10AM EDT in Room 204a.

http://www.advamed2010.com/go.cfm?do=Page.View&pid=80

Following the meeting, the presentation will be made available on the company’s investor relations website: http://www.cytosorbents.com/invest.htm

About AdvaMed 2010

AdvaMed 2010 is the premier MedTech conference for business leaders, entrepreneurs, policy-makers, media, financiers, and other industry stakeholders from around the world. In only its third year, AdvaMed 2009 attracted 1,400 industry leaders — including 500+ CEOs, Presidents and C-level executives. For more information, visit www.AdvaMed2010.com.

About CytoSorbents and CytoSorb™

CytoSorbents Corporation, and its operating subsidiary CytoSorbents, Inc., is a critical care focused therapeutic device company in clinical trials to treat severe sepsis, often called “overwhelming infection,” with a novel blood purification device called CytoSorb™. Severe sepsis afflicts more than 1 million people in the United States and an estimated 18 million people worldwide each year, killing one in every three patients despite the best treatment. In the United States, more die from severe sepsis than from either heart attacks, strokes or any single form of cancer. Severe sepsis is typically triggered by bacterial infections like pneumonia, or viral infections like influenza. However, it is the body’s abnormal immune response to the trigger that leads to severe inflammation and the unregulated, massive production of cytokines, often called “cytokine storm,” that then causes multi-organ failure and often death. CytoSorb™ is a cartridge containing highly porous polymer beads that are designed to filter cytokines and treat potentially fatal cytokine storm. As blood is pumped repeatedly through the CytoSorb™ cartridge using standard dialysis equipment, the beads bind and remove cytokines and other toxins from blood. The treated blood is then returned to the patient. The Company is currently conducting its European Sepsis Trial — a multi-center, randomized, controlled clinical trial using CytoSorb™ to treat up to 100 patients with severe sepsis in the setting of respiratory failure. Pending a successful trial, the Company will seek CE Mark approval and commercialization of CytoSorb™ in the European Union. Importantly, cytokine reduction via CytoSorb™ has broad applicability to a number of other critical care diseases where cytokine storm plays a detrimental role, including burn and smoke inhalation injury, trauma, acute respiratory distress syndrome, advanced influenza, acute pancreatitis and other. CytoSorb™ is one of a number of different resins designed for various medical applications, including improved dialysis, the potential treatment of inflammatory and autoimmune disorders, rhabdomyolysis in trauma, removal of chemotherapy during treatment of cancer with high dose regional chemotherapy, drug detoxification and others. Additional information is available for download on the Company’s website: www.cytosorbents.com

Forward-Looking Statements
This press release includes forward-looking statements intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Forward-looking statements in this press release are not promises or guarantees and are subject to risks and uncertainties that could cause our actual results to differ materially from those anticipated. These statements are based on management’s current expectations and assumptions and are naturally subject to uncertainty and changes in circumstances. We caution you not to place undue reliance upon any such forward-looking statements. Actual results may differ materially from those expressed or implied by the statements herein. CytoSorbents Corporation and CytoSorbents, Inc believe that its primary risk factors include, but are not limited to: obtaining government approvals including required FDA and CE Mark approvals; ability to successfully develop commercial operations; dependence on key personnel; acceptance of the Company’s medical devices in the marketplace; the outcome of pending and potential litigation; compliance with governmental regulations; reliance on research and testing facilities of various universities and institutions; the ability to obtain adequate financing in the future when needed; product liability risks; limited manufacturing experience; limited marketing, sales and distribution experience; market acceptance of the Company’s products; competition; unexpected changes in technologies and technological advances; and other factors detailed in the Company’s Form 10-K filed with the SEC on April 9, 2010, which is available at http://www.sec.gov.

Contact:

CytoSorbents Corporation
David Lamadrid
(732) 329-8885 ext. 816
[email protected]

Filed Under: Healthcare Policy and Law

REMINDER: Media Advisory: Suntron Grand Opening Event

Posted on October 5, 2010 Written by Editor

SOURCE: Suntron Corporation

METHUEN, MA–(Marketwire – October 5, 2010) – A ribbon cutting event is occurring at Suntron Corporation’s new manufacturing facility. Join Ed Wheeler, CEO of Suntron; Lt. Governor Timothy P. Murray; Congresswomen Niki Tsongas; Mayor Manzi III and Jose Bevilacqua in the opening event at 1pm, facility tour to follow.

Date:         October 5, 2010        
                                     
Time:         1:00 p.m.              
                                     
Location:     Suntron Corporation    
              300 Griffin Brook Drive
              Methuen, MA 01844      

For more information please contact:
Jen Winters
Email Contact
888-520-3382

Filed Under: Healthcare Policy and Law

Media Advisory: Suntron Grand Opening Event

Posted on September 30, 2010 Written by Editor

SOURCE: Suntron Corporation

METHUEN, MA–(Marketwire – September 30, 2010) –  A ribbon cutting event is occurring at Suntron Corporation’s new manufacturing facility. Join Ed Wheeler, CEO of Suntron; Lt. Governor Timothy P. Murray; Congresswomen Niki Tsongas; Mayor Manzi III and Jose Bevilacqua in the opening event at 1pm, facility tour to follow.

For more information please contact:
Jen Winters
Email Contact
888-520-3382

Filed Under: Healthcare Policy and Law

Suntron Corporation Announces Northeast Facility Grand Opening Event

Posted on September 30, 2010 Written by Editor

SOURCE: Suntron Corporation

METHUEN, MA–(Marketwire – September 30, 2010) –  Suntron Corporation, a leader in the area of integrated Electronics Manufacturing Solutions (EMS) and Commercial Off-The Shelf (COTS) technology, with facilities across the US and in Mexico, will cut the ribbon at its new manufacturing site in Methuen, MA at 1:00 PM, October 05, 2010.

This new facility is the culmination of months of effort to combine the work previously done in two separate sites, into a larger, newer, state of the art facility. “The move to combine our northeast services under one roof clearly demonstrates Suntron’s commitment to the region and to our customers,” Roger White, VP and General Manager of the Eastern Region, stated. “We have expanded our box build manufacturing footprint and with significant capital investment, we are expanding our circuit card capacity and capabilities. I look forward to introducing everyone to the exciting new facility.”

Mike Churchill, VP of Operations for Suntron, commented on the teamwork needed to put this together. “We had amazing cooperation from so many local people and organizations, including our team of realtors from Colliers Meredith and Grew, the City of Methuen, the local Merrimack Chamber of Commerce, and the Massachusetts Business Development and Business Services groups. Their total support and guidance allowed us to accomplish our objectives in a very timely manner and we look forward to introducing everyone to our exciting new facility.”

The grand opening and ribbon cutting ceremony will be hosted by Ed Wheeler, President and CEO of Suntron. Lt. Governor Timothy P. Murray, Congresswoman Niki Tsongas, Mayor William M. Manzi, III and Joe Bevilacqua, President and CEO of the Merrimack Chamber of Commerce will all participate at the event. Factory tours will begin immediately following the ceremony.

For further information on this event and the day’s agenda, please visit http://www.suntroncorp.com.

About Suntron Corporation:
Suntron delivers complete manufacturing services and solutions to support the entire life cycle of complex products in the medical, aerospace & defense, Industrial, Networking & telecommunications, and semiconductor capital equipment market segments. Headquartered in Phoenix, Suntron operates four full-service manufacturing facilities and two quick-turn facilities in North America. Suntron’s services include engineering services, printed circuit card assembly, box build, large scale and complex system integration, COTS and test.

For further information, please contact
Jen Winters
(602) 282-5242
Email Contact

Filed Under: Healthcare Policy and Law

CytoSorbents Corporation Achieves ISO 13485 Certification

Posted on September 27, 2010 Written by Editor

SOURCE: CytoSorbents Corporation

MONMOUTH JUNCTION, NJ–(Marketwire – September 27, 2010) –  CytoSorbents Corporation (OTCBB: CTSO), a critical care focused company using blood purification to treat life-threatening illnesses, announced the achievement of ISO 13485:2003 Full Quality Systems certification, a major milestone. ISO 13485 is an internationally recognized quality standard designed to ensure that medical device manufacturers have the necessary comprehensive management systems in place to safely design, develop, manufacture and distribute medical devices in the European Union (E.U.). It is a regulatory requirement of the E.U.’s Medical Device Directive and an important step toward attaining European CE Mark approval. 

Dr. Phillip Chan, Chief Executive Officer, stated, “We are very pleased to have attained this key milestone. ISO 13485 certification confirms that our manufacturing and quality systems meet the same high standards required of other major US medical device companies selling into Europe. Of the possible options, Full Quality Systems certification is the most stringent and efficient route to CE Mark approval for CytoSorb™ and other future CytoSorbents products. When coupled with CE Mark approval, ISO 13485 certification will allow CytoSorbents to commercialize its products in the E.U. market and other countries that recognize the ISO 13485 and CE Mark standards.”

About CytoSorbents and CytoSorb™

CytoSorbents Corporation, and its operating subsidiary CytoSorbents, Inc., is a critical care focused therapeutic device company in clinical trials to treat severe sepsis, often called “overwhelming infection,” with a novel blood purification device called CytoSorb™. Severe sepsis afflicts more than 1 million people in the United States and an estimated 18 million people worldwide each year, killing one in every three patients despite the best treatment. In the United States, more die from severe sepsis than from either heart attacks, strokes or any single form of cancer. Severe sepsis is typically triggered by bacterial infections like pneumonia, or viral infections like influenza. However, it is the body’s abnormal immune response to the trigger that leads to severe inflammation and the unregulated, massive production of cytokines, often called “cytokine storm,” that then causes multi-organ failure and often death. CytoSorb™ is a cartridge containing highly porous polymer beads that are designed to filter cytokines and treat potentially fatal cytokine storm. As blood is pumped repeatedly through the CytoSorb™ cartridge using standard dialysis equipment, the beads bind and remove cytokines and other toxins from blood. The treated blood is then returned to the patient. The Company is currently conducting its European Sepsis Trial — a multi-center, randomized, controlled clinical trial using CytoSorb™ to treat up to 100 patients with severe sepsis in the setting of respiratory failure. Pending a successful trial, the Company will seek CE Mark approval and commercialization of CytoSorb™ in the European Union. Importantly, cytokine reduction via CytoSorb™ has broad applicability to a number of other critical care diseases where cytokine storm plays a detrimental role, including burn and smoke inhalation injury, trauma, acute respiratory distress syndrome, advanced influenza, acute pancreatitis and other. CytoSorb™ is one of a number of different resins designed for various medical applications, including improved dialysis, the potential treatment of inflammatory and autoimmune disorders, rhabdomyolysis in trauma, removal of chemotherapy during treatment of cancer with high dose regional chemotherapy, drug detoxification and others. Additional information is available for download on the Company’s website: www.cytosorbents.com

Forward-Looking Statements
This press release includes forward-looking statements intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Forward-looking statements in this press release are not promises or guarantees and are subject to risks and uncertainties that could cause our actual results to differ materially from those anticipated. These statements are based on management’s current expectations and assumptions and are naturally subject to uncertainty and changes in circumstances. We caution you not to place undue reliance upon any such forward-looking statements. Actual results may differ materially from those expressed or implied by the statements herein. CytoSorbents Corporation and CytoSorbents, Inc believe that its primary risk factors include, but are not limited to: obtaining government approvals including required FDA and CE Mark approvals; ability to successfully develop commercial operations; dependence on key personnel; acceptance of the Company’s medical devices in the marketplace; the outcome of pending and potential litigation; compliance with governmental regulations; reliance on research and testing facilities of various universities and institutions; the ability to obtain adequate financing in the future when needed; product liability risks; limited manufacturing experience; limited marketing, sales and distribution experience; market acceptance of the Company’s products; competition; unexpected changes in technologies and technological advances; and other factors detailed in the Company’s Form 10-K filed with the SEC on April 9, 2010, which is available at http://www.sec.gov.

Contact:
CytoSorbents Corporation
David Lamadrid
(732) 329-8885 ext. 816
[email protected]

Filed Under: Healthcare Policy and Law

RecMan Releases World’s First Compliance and Records Management Software for Google Apps(TM)

Posted on September 20, 2010 Written by Editor

SOURCE: RecMan Inc.

Enables Millions of Additional Users to Flock to Google Apps Without Being in Violation of Compliance Standards

AUSTIN, TX–(Marketwire – September 20, 2010) –  RecMan Inc., today announced the availability of RecMan for Google Apps™, the world’s first web-based compliance and records management software designed to ensure policy and regulation compliance for millions of Google Apps™ users.

More than 20 million users within businesses, government agencies, schools and other organizations world-wide have switched to Google Apps. Unfortunately, many of them cannot use all of the applications within Google Apps since it does not have any built-in document compliance or records management features to meet organizational standards and legal regulations.

“By adding records management and compliance features to Google Apps, corporations, government and organizations of any size now have the ability to centrally apply document access control, retention and disposition policies. This enables compliance with HIPAA, Sarbanes Oxley, FERPA and other regulations, as well as internal policies,” says Richard Roberts, President and CEO of RecMan, Inc. “Records management and compliance features are usually only part of big expensive enterprise systems, but now those same capabilities are available in Google Apps for a fraction of the price.”

With the release of RecMan it can be expected that millions of additional users will flock to Google Apps, confident that they can be in full compliance with organization and government regulations.

On July 26, 2010 Google announced it was one of the first to receive certification and accreditation to provide cloud computing services to government agencies and private sector affiliations. Google is aware of the critical role that enterprise-grade records management and compliance occupies.

At the 2009 Gartner Symposium/ITxpo in Orlando, Eric Schmidt, CEO of Google, was asked how the company plans to meet compliance standards and regulations for information stored in the cloud. Schmidt responded that, “It’s time now for people to figure out how to take their business logic and connect it using our APIs to our underlying data stores,” thereby opening the door for third party vendors to help meet compliance needs.

The release of RecMan for Google Apps meets these needs and supports the three main standards for compliance and electronic records management including ISO 15489, DoD 5015.2 and MoReq2. RecMan for Google Apps enables records managers and compliance officers to easily and quickly apply organizational policies to all of the information stored in Google Apps.

RecMan for Google Apps meets five critical compliance needs espoused by ARMA International, the Association of Records Managers and Administrators, including a) centrally controlled document access management, b) document classification policy management, c) retention policy management, d) destruction and disposition policy management, e) legal hold management.

There is minimal training required to implement RecMan. Once the Records Manager or compliance officer sets up the policy information, users can drag and drop their document into the appropriate shared folder or choose it from the folder menu of Google Docs. The document then falls under the control of RecMan for Google Apps, enabling all of the access and retention policies of the organization to be applied automatically.

RecMan for Google Apps is available in the Google Apps Marketplace for $18 per user annually. It will also be available from a growing number of system integrators and resellers. For more information about RecMan for Google Apps, you can visit http://www.RecMan.net. 

About RecMan Inc.
RecMan Inc. is a venture funded start-up to provide world-class compliance and records management software. With offices in Austin, TX and Yokohama, Japan, RecMan was developed by Richard Roberts, the same designer that engineered the world’s first web-based compliance and records management software that is used by thousands of users world-wide. RecMan for Google Apps is the world’s first and only application that brings enterprise-grade records management and compliance to Google Apps.

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Filed Under: Health Technology and AI, Healthcare Policy and Law

APHL Commends U.S. Senate for Preserving New Health Reform Law: Threat to Unravel Prevention and Public Health Fund Defeated

Posted on September 20, 2010 Written by Editor

SOURCE: Association of Public Health Laboratories

SILVER SPRING, MD–(Marketwire – September 20, 2010) –  The Association of Public Health Laboratories (APHL) and its members commend the 52 Members of the United States Senate who on September 14 voted against the elimination of funding for the Prevention and Public Health Fund, which was created in the Affordable Care Act (ACA), the federal health reform law. This action assures that much-needed increases in federal support for public health laboratory operations will occur in federal fiscal years 2010 – 2015; jobs will be saved, surveillance and detection of harmful outbreaks will be increased and the health of Americans will improve.

Voting on a procedural matter (Roll Call Vote #231), the Senate rejected an amendment offered by Senator Mike Johanns (R-Nebraska) that would have used the resources in the Fund as an off-set on a matter wholly unrelated to the health of Americans.

In federal fiscal year 2010, the Fund will provide an increase in resources of almost fifty percent for activities that will improve the surveillance and detection of foodborne disease outbreaks and of emerging and re-emerging infectious disease outbreaks, while advancing the completeness of electronic health records. It is likely that the Fund will supply a doubling of funding for these activities in federal fiscal year 2011.

The significance of the eight-vote margin by which the amendment was defeated is greater when the extraordinarily strong push by the business community for the amendment is considered. Even in the face of this great success, the public health community nonetheless remains vigilant for the likely continuous attempts to siphon off the Fund for other uses and all other attacks to overturn the ACA and harm the health of Americans.

“The public health community came together quickly and cohesively in the effort to protect the Prevention and Public Health Fund from this attack,” said APHL Executive Director Scott Becker. “This accomplishment will be easily replicated for any future attempts to reduce or eliminate the Fund and should send a very clear message to those who seek other uses for it: ‘Hands Off!'”

The Association of Public Health Laboratories is a national non-profit located in Silver Spring, MD, that is dedicated to working with members to strengthen governmental laboratories with a public health mandate. By promoting effective programs and public policy, APHL strives to provide public health laboratories with the resources and infrastructure needed to protect the health of US residents and to prevent and control disease globally.

Contact:
Michelle M. Forman
Senior Media Specialist
240.485.2793
Email Contact

Click here to see all recent news from this company

Filed Under: Healthcare Policy and Law, Public Health and Research

National Healthcare Reform Conference Announces Finalized Agenda and Speakers to Discuss Future of Health Insurance Under Healthcare Reform Bill

Posted on September 14, 2010 Written by Editor

LOS ANGELES, CALIFORNIA–(Marketwire – Sept. 14, 2010) –

Editors Note: There is a photo associated with this press release.

The Top Healthcare and Health Insurance Leaders in the Nation will gather in Los Angeles at the National Healthcare Reform Conference, September 20-22nd, 2010, together to discuss the negatives and positives of healthcare reform and the challenges and, obstacles and the health reform bill will have on the health insurance and healthcare industry. Senior Leaders from health insurance companies, consulting firms, and healthcare providers will for the first time to discuss the upcoming implementation deadline of September 23rd for some of the new rules becoming effective under National Healthcare Reform. 

Jonathan Edelheit, Chairman of National Healthcare Reform Conference said, “It is indeed a great pleasure to see that leading employers, insurance companies, governmental entities, insurance agents and healthcare providers are all coming to the congress to find out how healthcare reform affects them and what new rules and regulations they need to comply with.” 

Many leading private and government organizations have expressed admiration on steps taken by Mr. Edelheit and his team to create such an important and extensive congress. As the congress is the dedicated gathering of experts on important subject.

The conference will address issues such as the new mandated minimum loss ratios, pre-existing condition clauses, new rules and regulations employers, insurance companies and healthcare providers must comply with. The healthcare reform congress will also address new mandated benefit for employees and insured.

“Bringing together a dynamic and diverse group of health care leaders, government officials and industry experts, this Conference will engender thoughtful and timely discussion about how the landscape of health care is changing. I am pleased to be a part of this important opportunity to address the challenges and implications of the health care law for all Americans,” said Therese Vaughan, CEO of the National Association of Insurance Commissioners (NAIC). 

Adding more to the topic Mr. Edelheit, also Editor-in-Chief of the Healthcare Reform Magazine added “Undeniably, without the up to date information, many employers and agents will find themselves in non-compliance with the new law, and will not be able to evaluate positive steps. Hence, I am content to see that Insurance leaders are gathering to discuss possible challenges, opportunities and issues related to the country’s growth.

National Healthcare Reform Conference is organized by the National Healthcare Reform Magazine, http://ww.healthcarereformmagazine.com, which is the only magazine and publication that addresses the effect, outcome and the future of healthcare reform. 

The finalized agenda is available at: http://healthcarereformconference.com/agenda.html.

The finalized list of speakers is available at: http://healthcarereformconference.com/speakers.html.

2010 National Healthcare Reform™ Conference Speakers are:

Brady Jensen, Group Manager, Global Benefits, Microsoft Corporation

Dr. Joseph P. Annis, Secretary, Board of Trustees, American Medical Association

Dr. Therese (Terri) Vaughan, Chief Executive Officer, National Association of Insurance Commissioners

Robert Moffit, Senior Fellow in Domestic and Economic Policy Studies, The Heritage Foundation

Cheryl Matheis, Senior V.P. Health Strategy, AARP

Terry K. Headley, President Elect, National Association of Insurance & Financial Advisors (NAIFA)

Stuart Barton, President, American Seniors Association

William (Bill) Barcellona, V.P. Government Affairs, California Association of Physicians Groups

Dr. Raymond Fabius, Chief Medical Officer, Healthcare & Science Business, Thomson Reuters

Michael Gibbons, Chairman, National Restaurant Association

Neil Trautwein, VP-Employee Benefits Policy Counsel, National Retail Federation

Christopher Khoury, Consultant, Head of Research Healthcare Practice, Gallup, Inc.

Melissa Boudreault, Director of Dell State Health Services, DELL

Brian N. Anderson, Consultant, Milliman, Inc.

Michael Bertaut, Senior Healthcare Intelligence Analyst, Blue Cross and Blue Shield of Louisiana

Janet Trautwein, Executive Vice President and CEO, National Association of Health Underwriters

Barry Hall, Principal, Buck Consultants

Devon M. Herrick, Senior Fellow, Ph.D., National Center for Policy Analysis (NCPA)

Lee D. Reichenbach, Market Manager, Hewitt Associates, West Coast Health Management Practice

Matt Hendrickson, MD, Vice Chair, PNHP, Physicians for National Health Program

Shelly Ten Napel, Senior Associate, State Coverage Initiatives, Academy Health

Craig Froude, President, WebMD Health Services

Eric D. Johnson, Regional Sales Manager, First Horizon Msaver

Rajiv Sabharwal, Chief Solutions Architect, Health & Life Sciences Practices, Infosys Technologies

Rob Thurston, President, HR Consulting Group

Ed Bray, Director of Compliance, Burnham Benefits Insurance Services

Andre Chasse, Director of Benefits, CoreLogic Inc., (Formerly The First American Corporation)

Kristi West, Sr. Manager, Benefits, SPHR-CA, GPHR,  Irvine Company

Kim Buckey, Compliance Lead, HighRoads

Denise Gott, VP of Sales,  LTC Financial Partners

Marcia Wagner, Principal, The Wagner Law Group

Greg Greenwood, PhD., MBA, President & CEO, Human Capital Specialists

David Ries, General Counsel, Human Capital Specialists

Andy Smith, M.D., Vice President/Chief Medical Officer, Saint Francis Memorial Hospital

Jeff Peters, President, Surgical Directions

Jean Patrick Tsang, President, Bayser Consulting

The National Healthcare Reform Conference is a stream of the Employer Healthcare Congress. http://www.employerhealthcarecongress.com . Together with four streams 1) Corporate Wellness Conference http://www.corporatewellnessconference.com 2)Voluntary Benefits and Limited Medical Conference http://www.voluntarybenefitsconference.com 3) Self Funding Employer Healthcare & Workers Compensation Conference http://www.selffundingconference.com and 4) the National Healthcare Reform Conference, The Employer Healthcare Congress is one of the largest US healthcare conferences in the country with over 1,000 attendees and up to 130 exhibitors and sponsors.

About the Healthcare Reform Magazine

The healthcare reform journal is a monthly publication focusing on how healthcare reform affects employers, insurers, insurance agents, healthcare providers and patients and will peel back the onion of the thousands of pages of healthcare reform bill to look at how different aspects of health care reform will really work.
http://www.healthcarereformmagazine.com.

To view the photo associated with this press release, please visit the following link: https://www.health-plan-news.com/wp-content/uploads/2010/09/d90c1a6dd8than08.jpg.jpg.

Filed Under: Healthcare Policy and Law

Virgin HealthMiles to Focus Healthcare Policy on Prevention at Prominent Fall 2010 National Conferences

Posted on September 14, 2010 Written by Editor

SOURCE: Virgin HealthMiles

Company Executives to Speak at Colloquy Loyalty Summit, World Congress 5th Annual Obesity and Wellness Congress, 2010 Integrated Care Summit and 2nd Annual Retail Health Clinics Congress

BOSTON, MA–(Marketwire – September 14, 2010) –  Rising healthcare costs. Confusing healthcare reform policies. Under-utilized wellness programs. These are just a few reasons why HR executives, healthcare industry leaders, and policy makers seek insight from industry-leading providers with first-hand experience in how to make employee health and wellness programs effective and measurable. Virgin HealthMiles is at the forefront providing strategic guidance and practical steps to implement and sustain effective employee health programs.

Continuing in their thought leadership roles, Virgin HealthMiles CEO Chris Boyce and President Sean Forbes share their perspectives about the role of prevention in employee health programs at four national industry conferences this fall.

Forward-thinking businesses recognize that costly and preventable lifestyle-driven behaviors have the potential to spark a profitability crisis of epic proportions for U.S. companies. Healthcare costs are expected to rise by about 8.9 percent in 2011, according to a National Business Group on Health report released in August, continuing the trend seen in recent years. What’s more, 85 percent of companies believe simply extending insurance to Americans, a key feature of the new health reform legislation, won’t make individuals healthier, according to a recent study conducted by Virgin HealthMiles in conjunction with Workforce Management magazine. Insurance alone won’t solve the problem of preventable, lifestyle-related disease. Consider that chronic disease — the majority of which are preventable — account for 75% (or $1.5 trillion) of healthcare costs impacting businesses and their employees today. Keeping people healthy and out of the healthcare system in the first place will have the most significant impact on costs.

During the upcoming conferences, Boyce and Forbes will draw from their experiences working with more than 120 U.S. companies to engage employees to be active and healthy, and will share insights on why a new generation of prevention is key to helping corporate America get ahead of rising healthcare costs. Virgin HealthMiles’ Pay-for-Prevention™ approach has helped companies create a culture of health, align their interests with those of their employees, and design incentives for healthy behaviors. Results include above industry-average employee engagement levels, improvements in employee health, and decreases in rising healthcare costs. 

Details of each conference follow:

2010 Colloquy Loyalty Summit in Phoenix, Arizona
September 16
th at 3:30-4:15 p.m.
“Feeling Better – Using Loyalty Recognition and Rewards to Improve Wellness” 
http://www.colloquy.com/2010-summit-agenda.htm
Boyce will participate in a panel discussion on how loyalty programs are being applied to wellness, and how they can motivate employees to live healthier lives and reduce healthcare costs.

World Congress’ 5th Annual Obesity and Wellness Congress in Washington D.C.
September 30
th at 3:25-4:40pm
“Worksite Wellness – Why Employers Should Address the Obesity Epidemic”
https://www.worldcongress.com/agenda.cfm?level=inside&confCode=HL10088&agendaID=532&subAgendaID=1336
Forbes will participate in the closing key-note panel discussion on how to overcome employee resistance and facilitate positive behavior change with incentives to address the obesity epidemic. He will also address the “carrot versus stick” approach and creative strategies for motivating employee participation in employee health programs.

2010 Integrated Care Summit in Washington D.C.
October 15
th at 10:00-11:00 a.m.
“Creating a Culture of Prevention: Designing an Integrated Approach to Employee Health That Delivers Measureable Results”
http://www.dmaa.org/ics10/program_track4.asp
Boyce will discuss how creating a culture of prevention aligns the interests of companies and their employees to lower healthcare costs. He will also discuss wellness measurement strategies.

2nd Annual Retail Health Clinics Congress in Las Vegas, Nevada
October 25
th at 1:45-2:30 p.m.
“Retail Health Clinics and their Role in Employer Health and Wellness”
http://www.globalmediadynamics.com/upcoming-events/retail-health-clinics
Boyce will provide insight on how retail health clinics can directly bolster employee health and wellness programs. He will also discuss how to effectively utilize biometric data and other resources in order to measure and manage program effectiveness.

About Virgin HealthMiles
Virgin HealthMiles provides employee health programs that pay people to get active. The company’s Pay-for-Prevention™ approach, based on physical activity and healthy lifestyle change, attracts an average of 40 percent of employees who participate, which helps organizations reduce medical costs and improve employee productivity and satisfaction. The program is offered by employers, government entities, and insurers. Over 120 industry leaders representing more than 500,000 employees across the U.S., including American Diabetes Association, Intuit, MWV, OhioHealth, Ochsner Health System, Protective Life, SunGard, SunTrust, and Timberland have selected Virgin HealthMiles’ award-winning program for their employees. The company is a member of Sir Richard Branson’s Virgin Group. For more information, visit www.virginhealthmiles.com

Media Contact:
Kathy Wilson
Email Contact
781-652-0499

Click here to see all recent news from this company

Filed Under: Healthcare Policy and Law

Care Share Providing Three Days of Learning & Collaboration for NC Health Care Safety Net Partners

Posted on September 8, 2010 Written by Editor

SOURCE: Care Share Health Alliance

Regional Workshops Feature Health Reform, Local Successes and the Funders’ Perspective

RALEIGH, NC–(Marketwire – September 8, 2010) –  Care Share Health Alliance is gathering some of the best health care minds in the state and bringing them together for three interactive meetings across North Carolina this fall. These sessions will provide North Carolina safety net partners with the opportunity to:

  • interact with state and local leaders on best practices in developing collaborative networks of care;
  • hear how health reform may affect them and the safety net;
  • learn from state, regional and local funders how to effectively work with funders during these challenging economic times.

The meetings are open to the public and targeted toward those who provide health care services to low-income uninsured populations, or those who are involved in guiding or navigating the uninsured to resources for care. This includes, but is not limited to, anyone involved with organizations such as: hospitals, community health centers, Federally Qualified Health Centers, rural health centers, health departments, free clinics, HealthNet networks, departments of social services, medical societies, dental societies, Area Health Education Centers, behavioral health organizations and other nonprofit agencies. 

“We chose to hold three regional meetings instead of one statewide meeting to make these workshops as convenient as possible for safety net partners and to make the content as locally relevant as possible,” says Care Share Executive Director Kellan Chapin. “Participants will get to hear from state health care leaders, but will also get to interact with their regional colleagues and learn from each other.”

Sessions take place:

  • Friday, Sept. 24 in Asheville
  • Tuesday, Oct. 5 in Greenville
  • Thursday, Oct. 21 in Greensboro

The workshops run 9 a.m. to 4 p.m. and a $50 registration fee covers workshop supplies, a light continental breakfast, lunch and other refreshments.

The Asheville workshop features Karen Minyard, director of the Georgia Health Policy Center, discussing health care reform. The Greenville session features Pam Silberman, president of the North Carolina Institute of Medicine, on health care reform, and Tami Eldridge, Scott Whisnant and Sheila Roberts from Cape Fear HealthNet on tools and best practices for building collaboration among safety net partners. And the Greensboro meeting features: Dr. Robert Strack, head of the Department of Public Health Education at UNC Greensboro discussing a community approach to improving health; psychologist Dr. Doris Paez of NC State University on tools and best practices for collaboration building; and attorney Alicia Gilleskie of Smith Anderson discussing HIPAA, the Health Insurance Portability and Accountability Act, and tools for sharing data.

Register and get more information at www.caresharehealth.org or call 919-861-8353.

About Care Share
Care Share is a 501(c)3 nonprofit, statewide resource that helps communities develop comprehensive networks to coordinate care for low-income uninsured and underserved populations. Care Share helps communities by: bringing people together to create a shared plan for serving those in need; sharing knowledge and resources within communities; and sharing best practices and guidance among communities across the state.

Assistance is available to communities throughout the state at no charge. Call 919-861-8353 for more information.

Contact:
Linda Kinney, MHA
Director, Collaborative Network Development
Care Share Health Alliance
(919) 861-8356
Email Contact

Kellan Chapin, MPH
Executive Director
Care Share Health Alliance
(919) 861-8357
Email Contact

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Filed Under: Healthcare Policy and Law

Virgin HealthMiles to Examine Role of Prevention in New Healthcare Legislation During Free Webinar

Posted on September 8, 2010 Written by Editor

SOURCE: Virgin HealthMiles

BOSTON, MA–(Marketwire – September 8, 2010) –  Virgin HealthMiles, a leading provider of employee health and productivity programs that reward individuals for getting healthy, today announced it will host a free webinar focused on the role of prevention in the new healthcare reform legislation and how organizations can obtain measurable business value from their healthcare decisions.

The webinar, “Healthcare Reform: The Role of Prevention in the New Legislation,” will be held Tuesday, September 14, 2010, from 2:00 p.m. – 3:00 p.m. ET. 

Virgin HealthMiles President Sean Forbes will be joined in the webinar by Brian Klepper, an expert on healthcare reform. Klepper is an Aspen Institute Health Forum Fellow and serves as one of only three non-physicians on the International Editorial Board of the Medscape Journal of Medicine. He is also a health care columnist for American City Business Journals and writes for The Health Care Blog.

During this webinar, the presenters we will take a strategic and tactical look at the role of wellness in the Patient Protection and Affordable Care Act (PPACA), including:

  • A high-level summary of the PPACA with a focus on the wellness provisions
  • A chronological look at the impact of reform on business
  • How to obtain measurable business value from a company’s healthcare decisions

To register for the live webinar, please visit:
https://event.on24.com/eventRegistration/EventLobbyServlet?target=registration.jsp&eventid=239510&sessionid=1&key=1A9E973CA1C8590F6C3EEBEE02EAEB02&partnerref=VHMPress

A free recording of the webinar will be available on the Virgin HealthMiles website at: www.virginhealthmiles.com. 

About Virgin HealthMiles
Virgin HealthMiles provides employee health programs that pay people to get active. The company’s Pay-for-Prevention™ approach, based on physical activity and healthy lifestyle change, attracts an average of 40 percent of employees who participate, which helps organizations reduce medical costs and improve employee productivity and satisfaction. The program is offered by employers, government entities, and insurers. Over 120 industry leaders representing more than 500,000 employees across the U.S., including American Diabetes Association, Intuit, OhioHealth, Ochsner Health System, MWV, Protective Life, SunGard, SunTrust, and Timberland have selected Virgin HealthMiles’ award-winning program for their employees. The company is a member of Sir Richard Branson’s Virgin Group. For more information, visit www.virginhealthmiles.com

Media Contact:
Kathy Wilson
Email Contact
781-652-0499

Click here to see all recent news from this company

Filed Under: Healthcare Policy and Law

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