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ProView Plus Print Generic Pharmaceutical Patent and FDA Law

Product details:

Format: Book and Electronic
Brand: Thomson West
Copyright: 2022
Service #: 30920680
Sub #: 30924444
Publication Frequency: Updated as changes in the law dictate
Update format: N/A

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ProView Plus Print Generic Pharmaceutical Patent and FDA Law



In stock

Book and Electronic
Special pricing applies

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: Provides step-by-step process for understanding, strategizing, and litigating generic drug patent infringement Provides comprehensive background in patent and (FDA) regulatory law, integrating them into one cohesive bundle Dissects each complex issue into its parts and cross-references it to other issues Provides an excellent teaching tool for associates, partners, law clerks, judges, and financial managers Provides case studies, illustrations, and timelines Covers the generic drug industry exclusively, blending generic drug patent and FDA issues Offers citations to cases