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November 9-11, 2020 | Virtual Conference
David Rosen is a partner and FDA/public policy lawyer with Foley & Lardner LLP. Mr. Rosen has extensive experience in health law, life sciences, and food and drug regulation, including a range of Food and Drug Administration (FDA) regulatory issues affecting prescription and over-the-counter pharmaceuticals, medical devices, biologics, dietary supplements, foods, cosmetics and tobacco products. He is co-chair of the firm’s Life Sciences Industry Team, FDA Practice Group Leader and is also a member of the firm’s Government & Public Policy Practice and the Health Care and Food & Beverage Industry Teams.
Mr. Rosen was formerly a partner with two other law firms. He was also employed by the FDA for 14 years, progressing to various supervisory positions involving virtually all aspects related to the drug approval process, combination products, jurisdictional issues and related compliance activities.
Mr. Rosen has been Peer Review Rated as AV® PreeminentTM, the highest performance rating in Martindale-Hubbell’s peer review rating system. In 2012 – 2014, The Legal 500 recognized Mr. Rosen for his work in life sciences. He has been a frequent speaker before national and international pharmaceutical industry associations on the ANDA submission and review process and on the IND and expedited drug development, review, and approval processes. Mr. Rosen has made presentations before investment analysts and managers of venture capital on the impact of FDA on the drug and biotech industry.
Mr. Rosen is an emeritus member of the University of Connecticut School of Pharmacy Advisory Board.
Mr. Rosen earned his J.D. at The Catholic University of America, Columbus School of Law (1991). He also holds a Bachelor of Science degree from the University of Connecticut School of Pharmacy (1978).