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Generic Pharmaceutical Patent and FDA Law, 2012 ed.

Generic Pharmaceutical Patent and FDA Law, 2012 ed. New Edition

By Shashank Upadhye
Copyright: 2012
ISBN-13: 9780314607539
Last Updated: 3/9/2012
Availability: In Stock  
Product Details »
Brand: Thomson West
Pages: 1054
Components: 1 Print
Shelf Space: 2 in.
Free Update Period: 90 days
Shipping: FREE Ground Shipping »
Free ground shipping is available on every in-stock West order shipped within the United States. If you choose this option, your order will generally ship from West within 1-2 business days and arrive within 7-10 days via the carrier that West selects. Past-due accounts and other credit issues may delay your order.
Available Options:
Book - softbound
List Price:
 $379.00
Monthly book pricing (What's This? )
Monthly Book Pricing through the Assured Print Pricing Service allows you to budget your purchase and updates evenly across 12 months. Contract options are for 24 or 36 months and include all updates.

Description

This practitioner's guide walks the practitioner 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 discusses the areas that impact the interaction of patents and Food and Drug Administration law, including litigation.

Features

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

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