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The Weinberg Group is a Washington, DC–based food and drug regulatory consulting group. Founded in 1983, the firm assists pharmaceutical and biotech companies with the "development and implementation of successful and innovative regulatory strategies" and also helps these companies to "remediate, maintain and improve their regulatory compliance."
FDA Building 32 houses the Office of the Commissioner and the Office of Regulatory Affairs. The Office of Global Regulatory Operations and Policy (GO), [1] also known as the Office of Regulatory Affairs (ORA), [2] is the part of the U.S. Food and Drug Administration (FDA) enforcing the federal laws governing biologics, cosmetics, dietary supplements, drugs, food, medical devices, radiation ...
LOGOS GmbH, a provider of regulatory services to pharmaceutical manufacturers, for $3.9 million in own common stock. [ 18 ] March 1999: Parexel acquires Groupe PharMedicom S.A. , a French provider of post-regulatory services to pharmaceutical manufacturers, based in Paris and Orléans and employing approximately 70 people, in exchange for ...
The Reagan-Udall Foundation for the Food and Drug Administration is a private nonprofit (501c3) organization, created to support the mission of the U.S. Food and Drug Administration (FDA) to help equip FDA staff with the highest caliber, regulatory science and technology in order to enhance the safety and effectiveness of FDA regulated products.
Regulatory affairs (RA), is a profession that deals with an organization’s adherence to regulatory compliance.. It is a position mostly found within regulated industries, such as pharmaceuticals, medical devices, cosmetics, agrochemicals (plant protection products and fertilizers), energy, banking, telecom etc. Regulatory affairs also has a very specific meaning within the healthcare ...
The Center for Food Safety and Applied Nutrition (CFSAN (/ ˈ s ɪ f ˌ s æ n / SIF-san)) is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements, and cosmetics, as opposed to drugs, biologics, medical devices, and radiological products, which also fall under the purview of the FDA. [3]
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