Popular Articles

Rotherham Nurse Raises Alarm Over Infant Medicine Feeder
A concerned Rotherham nurse has forced manufacturers of an infant medicine feeder to withdraw its product following a safety scare. Nurse Karen Ray, a clinical procurement specialist at Rotherham Hospital, took her concerns to the Medicines and Healthcare products Regulatory Agency (MHRA) after a six-month-old baby was admitted to Rotherham Hospital following a liquid paracetamol overdose.

HANYS Presents Its Top Honor, The Distinguished Service Award, To New York State's Health Care Auxilians
Hundreds of health care leaders from throughout the state gathered Wednesday evening in Lake George as the Healthcare Association of New York State (HANYS) presented its 30th annual Distinguished Service Award, its highest honor, to New York State"s health care auxiliaries. Since 1979, HANYS has awarded the Distinguished Service Award to individuals who demonstrate their extraordinary commitment to improving health care through service to their community.
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MPS Clarifies Indemnity Arrangements For GPs During A Pandemic Flu Outbreak
Medical Protection Society (MPS) GP members, who are expected to work outside of their normal duties during a pandemic flu, should feel confident that they can turn to the MPS for assistance, in the event they are subject to a clinical negligence claim or other medicolegal matter such as a complaint.
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AARP Biologics Study Based On Fuzzy Math, Flawed Assumptions

The following statement was issued by the Biotechnology Industry Organization (BIO) regarding a study on biosimilars presented to Congressional staff by the AARP: "The so-called AARP "study" is simplistic, misleading and extremely flawed. It is based on fuzzy math and even fuzzier assumptions. "The study cherry picks the best selling biologic products to draw erroneous conclusions, ignoring the bulk of the biologics market. The real facts show that only a small percentage of biotechnology products have the types of financial returns identified in the AARP study. If AARP had analyzed all of the more than 200 other FDA-approved biologics they conveniently left out of their fact sheet, their analysis would have reached a much different, and more credible, result. That"s because the "break even" point for all the other FDA-approved biologics approaches 50 years. "Greater than 90% of biologic products fail before even getting to clinical trials. Of those entering clinical trials, only 30% get approved by FDA. Of those approved products, only 34% generate profits equal to or greater than the development cost over the product"s lifecycle. "As one of the nation"s largest insurance providers, AARP has a lot to gain financially by using its considerable lobbying muscle to push Congress to pass biosimilars legislation that will benefit insurers by providing short-term cost savings at the risk of jeopardizing the continued development of advanced and breakthrough medicines and cures for patients. Biotechnology medicines extend and improve the quality of life - and provide renewed hope - for patients suffering from debilitating diseases such as cancer, HIV/AIDS, Parkinson"s, Multiple Sclerosis, diabetes and a host of rare diseases. "Congress should not develop public policy based on such a flawed and blatantly biased analysis. Now is the time to implement a pathway to biosimilars that safely increases access to the breakthrough therapies and cures for the patients of today, while preserving the incentives necessary to address the unmet medical needs of the patients of tomorrow." BIO


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