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Generic Pharmaceutical Patent and FDA Law covers Food and Drug Administration (FDA)approval of generic drugs and the interaction of patents and FDA law. A practitioner's guide, it walks the reader through the stages of drug approval, identifying the critical issues in the process and advising the client about the issues and areas of concern or exploitation. It also discusses the areas that impact the interaction of patents and Food and Drug Administration law, including litigation. Features of this publication include:
Enter replacement volume, chapter and page numbers separated by commas. For example: Volume 2, Chapter 5, Pages 7, 12-19. Please limit requests to 25 pages or less. If you are located outside the United States or for more than 25 pages please contact Customer Service 1-800-328-4880.
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