October 4, 2018
Life Science Leader
By Michael J. Flibbert; Megan Leinen Johns
If you read part one of this series, you appreciate that it is imperative that all individuals involved in drug development — including scientific, regulatory, marketing, and financial personnel — understand how their activities may affect obtaining and maintaining patent coverage in future actions to preserve U.S. market exclusivity. Indeed, anyone having reason to comment on topics potentially relevant to enforcing patents, particularly those listable in the FDA’s Orange Book, can benefit from a better understanding of patentability requirements and how patent protection might be challenged. In this article Finnegan attorneys discuss how to prepare a drug candidate for ANDA litigation
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Originally printed in Life Science Leader on October 4, 2018. This article is for informational purposes, is not intended to constitute legal advice, and may be considered advertising under applicable state laws. This article is only the opinion of the authors and is not attributable to Finnegan, Henderson, Farabow, Garrett & Dunner, LLP, or the firm's clients.
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