PCAB Executive Stepping Down
PCAB Executive Director Tom Murry, PharmD, Esq, is stepping down effective December 31, 2010. Tom Murry won election to a seat in the North Carolina State House and will be a part-time owner of a community pharmacy in Raleigh, North Carolina. During the past 3 years, PCAB has nearly doubled, now has 100 accredited pharmacies, and that number is increasing.
PCAB is a not-for-profit corporation formed by eight national pharmacy organizations recognizing the need for a national standards organization for compounding pharmacies. More information can be obtained at: http://www.pcab.org
India and China Pharmaceutical Industry to Cooperate to Increase Generic Drugs Supply in World
Aiming to become major global pharma players, Indian and Chinese pharmaceutical industries have agreed to collaborate in supplying generic drugs to the world. A memorandum of understanding (MOU) is scheduled to be signed between Indian Drug Manufacturer's Association (IDMA) and China Pharmaceutical Industry Association (CPIA) in Mumbai on January 7.
The purpose of the MOU is to provide information, data, and guidance to each other's members regarding topics such as regulations, registration, importation, distribution, marketing, and administration of drugs and medicines. This collaboration will give an edge over the developed countries, and together they have stated they can meet the generic drugs requirements of the world.
http://www.business-standard.com/india/news/india-china-pharma-bodies-to-sign-cooperation-pact/119335/on
FDA Issues New Warning on Illegal Supplements
The FDA has issued a new warning about some dietary supplements and bodybuilding and sexual enhancement products in a letter asking manufacturers and trade groups to help police the growing industry.
In recent years, the FDA has issued nearly 300 alerts about dietary supplements alone, including those containing sibutramine, the active ingredient in the drug Meridia (which was withdrawn from the market by Abbott Laboratories in October due to heart attack and stroke risks).
Dietary supplements do not have to be approved by the FDA for safety or effectiveness before marketing, and the manufacturers can make general claims about health or well-being; however, they are not supposed to claim to prevent or cure specific diseases. Supplements may be considered adulterated, unsafe, and illegal if they include some prescription drug chemicals. The three most common types of illegal supplements include weight-loss, body-building, and sex enhancer products.
http://prescriptions.blogs.nytimes.com/2010/12/15/f-d-a-issues-new-warning-on-illegal-supplements/?partner=rss&emc=rss
EPA Takes Saccharine Off Hazardous Substance List
The EPA has removed saccharine from its list of hazardous substances. It is no longer considered a potential hazard to human health. Saccharin was labeled a potentially cancer-causing substance in the 1980s.
The National Toxicology Program and the International Agency for Research on Cancer re-evaluated the available scientific information on saccharin in the late 1990s and concluded it is not a potential human carcinogen.
http://www.upi.com/Science_News/2010/12/14/EPA-takes-saccharine-off-hazardous-list/UPI-57841292374416/
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