Skip to content Skip to navigation menu
Your browser is not supported by this site.
Please update to the latest version, or use a different browser for the best experience.
Generic Pharmaceutical Patent and FDA Law, 2018-2019 ed.

Product details:

Format: Book - softbound
Brand: Thomson West
Copyright: 2018
ISBN: 9780314895301
Service #: 40614278
Sub #: 40614279
Pages: 1360
Shelf Space: 1 in.
Publication frequency: Updated annually
Update method: Replacement pamphlets

Can we help?

Contact Us 
Call 1-888-728-7677

Generic Pharmaceutical Patent and FDA Law, 2018-2019 ed.



In stock

One time purchase
Purchase the current version only, no updates will be sent.

Monthly pricing
Convenience of fixed monthly payments and long term price protection. Choose 24 or 36 months. All updates, revisions, and new editions included.

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