2018-03-23T05:50:24
Section 510 of the Federal Food, Drug, and Cosmetic Act (FD& C Act) requires firms that manufacture, prepare, propagate, compound, or process drugs in the U.S. or that are offered for import into the U.S. to register with the FDA. These domestic and foreign firms must at the time of registration, list all drugs manufactured, prepared, propagated, compounded, or processed for commercial distribution in the U.S. Additionally, foreign establishments must identify a U.S. agent and importers at the time of registration.
DCGI, CDSCO, Drug, Medical Device, cosmetic Registration/ license Consultant in India
Drug Regulatory Services India
Drug and cosmetic Act
Drug Regulations India
Drug Registration Delhi
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