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FDA News Release

FDA announces Pharmacy Compounding Advisory Committee members

For Immediate Release

December 16, 2014


The U.S. Food and Drug Administration today announced the membership of the Pharmacy Compounding Advisory Committee. The committee is comprised of 14 members  - 12 voting and two non-voting - who will provide advice on scientific, technical and medical issues concerning drug compounding under sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act.

 “Advisory committees are a very important source of knowledge and advice for drug regulation,” said Janet Woodcock, M.D., director of the FDA’s Center for Drug Evaluation and Research. “This is a key step toward implementing the compounding provisions of the Drug Quality and Security Act, and I expect we will benefit greatly from the advice and recommendations the members of the committee provide.” 

The members are experts in pharmaceutical compounding and manufacturing, pharmacy, medicine, and pharmaceutical regulation. The FDA solicited nominations for committee members, and more than 100 individuals were nominated. The FDA also identified some qualified candidates from its own pool of special government employees.

The committee includes voting members representing the United States Pharmacopeia (USP), a nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines manufactured, distributed and consumed worldwide; the National Association of Boards of Pharmacy (NABP), a professional organization that supports the state boards of pharmacy in protecting public health; and one member identified with consumer interests. Two non-voting members represent the pharmacy compounding industry and the pharmaceutical manufacturing industry. 

Candidates not representing a particular group were evaluated for conflicts of interest and to determine whether their qualifications matched the required areas of expertise.

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.




 Christopher Kelly



Page Last Updated: 12/16/2014
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