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Lee H. Rosebush, Associate
- 202-739-5153
- lrosebush@morganlewis.com
- www.morganlewis.com
Lee H. Rosebush is an associate in Morgan Lewis’s FDA and Healthcare Practice. His practice focuses on FDA regulatory, compliance, and enforcement issues pertaining to pharmaceuticals, biologics, and medical devices. Dr. Rosebush has also appeared before state boards of pharmacies and has assisted clients with various issues related to Medicare, Medicaid, and state regulatory requirements, including state licensing requirements, for healthcare providers and pharmacies, as well as drug and device manufacturers and distributors. As part of his practice, Dr. Rosebush regularly provides regulatory counsel to pharmaceutical, medical device, and dietary supplement manufacturers; advises clients in matters relating to FDA regulatory compliance, including governance in the drug naming process, clinical trial, marketing, promotion and advertisement, and approval process; and advises private equity, public, and private companies in transactional matters. In addition, he has authored an amicus brief for a matter before the U.S. Supreme Court.
- Morgan, Lewis & Bockius LLP
Articles in the National Law Review database by Lee H. Rosebush:
- FDA Requests Comments on the Development of a User Fee Program for Biosimilar and Interchangeable Biological Products (Posted On Tuesday, May 24, 2011)
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