0
Thanks

A few words of thanks would be greatly appreciated.

Regulation of therapeutic goods - Definition


Definition


Regulation of therapeutic goods is carried out by the U.S. Food and Drug Administration, or F.D.A., for all medical and veterinary products placed on the market. Authorization of a product takes into account the benefits and the risks associated with the consumption of the drug. The request for authorization consists of thousands of pages detailing the studies carried out on the drug, especially on its chemical properties, its beneficial effects, its undesirable effects, and the processes of its manufacturing.
0
Thanks

A few words of thanks would be greatly appreciated.

Ask a question
CCM is a leading international tech website. Our content is written in collaboration with IT experts, under the direction of Jeff Pillou, founder of CCM.net. CCM reaches more than 50 million unique visitors per month and is available in 11 languages.

Related

0 Comments