ACI's 35th FDA Boot Camp

March 24 - 25, 2020 - NY US

American Conference Institute


Having a strong grasp of vital FDA regulatory protocols to bring a pharmaceutical or biological product to market, from the pre-approval to post-approval processes remains essential for attorneys, regulatory professionals and executives within the life sciences industry. Recent agency actions and highly publicized trials related to FDA regulated products only furthers the need to have an in-depth understanding of such fundamental FDA concepts as NDAs, BLAs, product labeling, clinical trials, adverse events reports, patent concerns, and exclusivity. ACI’s FDA Boot Camp returns to New York for its 35th edition. with the intention of providing life sciences legal professionals and executives with a working knowledge of essential FDA concepts, and real-world examples that will guide them in their everyday practice.

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