An Overview of FDA's Patent Listing Process U.S. Food and Drug Administration 12:30 3 years ago 1 317 Далее Скачать
Orange Book 101: An Overview of FDA's Orange Book U.S. Food and Drug Administration 24:05 3 years ago 5 462 Далее Скачать
FDA Drug Info Rounds, July 2012: Patents and Exclusivity U.S. Food and Drug Administration 3:20 12 years ago 17 354 Далее Скачать
Changes to Orange Book Patent Information U.S. Food and Drug Administration 52:54 3 years ago 3 962 Далее Скачать
Importing FDA-Regulated Products: The Import Process U.S. Food and Drug Administration 10:55 2 years ago 50 423 Далее Скачать
How does the FDA approve new drugs? U.S. Food and Drug Administration 3:17 1 year ago 57 256 Далее Скачать
Para four filing procedure, and 180 days Exclusivity Pharma Learners 5:50 6 years ago 17 179 Далее Скачать
The Patent Information Dispute Process U.S. Food and Drug Administration 28:20 3 years ago 484 Далее Скачать
Timeline for the Drug Master Review Process U.S. Food and Drug Administration 22:08 3 years ago 4 413 Далее Скачать
Orange Book: 101 An Overview (11of27) Generic Drugs Forum 2018 U.S. Food and Drug Administration 16:56 4 years ago 1 469 Далее Скачать
Components of New Drug Application and Biologics License Application (5of15) REdI– May 29-30, 2019 U.S. Food and Drug Administration 36:55 4 years ago 12 665 Далее Скачать
How does the FDA approve new drugs? U.S. Food and Drug Administration 3:17 10 months ago 4 147 Далее Скачать
Overview of the FDA Product-Specific Guidance Program U.S. Food and Drug Administration 13:21 3 years ago 1 536 Далее Скачать
Generic Para IV Certification (Patent Challenge) Exclusivity PHARMA INDUSTRY TRAINING EDUCATION 10:38 1 year ago 4 586 Далее Скачать
Orange Book Exclusivity: An Introduction and Overview U.S. Food and Drug Administration 12:36 3 years ago 1 870 Далее Скачать
The FDA Drug Development Process: GLP, GMP and GCP Regulations GlobalCompliance Panel 1:31:06 8 years ago 98 827 Далее Скачать