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Pharmaceutical Patent Law, Third Edition with 2018 Supplement


By Jesse Schwartz
Published: October 3rd, 2018

Pharmaceutical Patent Law, Third Edition takes on the complicated tasks of tracking legal developments within the Patent and Trademark Office, the FDA, Congress, the courts, the FTC, the Department of Justice, and the World Trade Organization; examining how these agencies and organizations interact with each other; and determining how they impact patent and IP protection strategies. This 900+ page treatise is the only reference available with a detailed, practitioner-oriented treatment from the perspective of both patent law and food and drug laws.

Pharmaceutical Patent Law provides complete coverage of advanced topics, including the antitrust implications of patent settlements, the experimental use privilege, and international IP and regulatory challenges. Core topics covered include follow-on biologics; the substance and procedure of pharmaceutical patent acquisition; FDA marketing approval procedures for innovative and generic drugs, as well as FDA marketing exclusivities; the FDA’s Orange Book; and patent term extension standards.

For complete details, CLICK HERE.

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