1. Introduction to pharmaceutical patents; 2. Patent eligibility; 3. Utility; 4. Novelty; 5. Nonobviousness; 6. The patent instrument; 7. Patent acquisition procedures; 8. Duration of rights; 9. The FDA drug approval process; 10. The orange book; 11. Marketing exclusivities; 12. Scope of patent rights; 13. Claim interpretation and the doctrine of equivalents; 14. Parallel importation; 15. The experimental use privilege; 16. Antitrust considerations; 17. International and comparative patent law; 18. International and comparative data protection law.
Introduction to pharmaceutical patents Patent eligibility Utility Novelty Nonobviousness The patent instrument Patent acquisition procedures Duration of rights The FDA drug approval process The orange book Marketing exclusivities Scope of patent rights Claim interpretation and the doctrine of equivalents Parallel importation The experimental use privilege Antitrust considerations International and comparative patent law International and comparative data protection law.
Published
Washington, D.C. : Bureau of National Affairs, 2005.