Free Seminar on the FDA Process for Approving Generic Drugs
Click here for the U.S. Food and Drug Administration's free, December 2004 video, online training seminar on "The FDA Process for Approving Generic Drugs," from the Center for Drug Evaluation and Research.
The seminar provides viewers with an overview of the Food and Drug Administration's role in the generic drug process, including various aspects of the Abbreviated New Drug Application (ANDA) process, the "Orange Book," and the complexities of the patent certification process and its impact on the approval of generic drug products.
The estimated completion time for this video is 60 minutes.
2 Comments:
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That is an awesome seminar. Thanks so much for sharing this video to your readers. The truth is, I have been searching the web about the FDA's process of approving generic drugs. I believe with our application of near infrared technology in our manufacturing process, consistency in all the raw materials is guaranteed. Personally, I think the NIR technology is truly a blessing for many pharmaceutical companies.
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