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FDA approval is necessary to bring a new medical device of drug to market. The question many of us ask is this: Why is it so difficult?
Bob Seevers is a senior advisor with Pearl Pathways and has devoted 24 years of his professional life working with the FDA, eight of them as an FDA team leader, managing a team of reviewers. Today, he advises companies on how to expedite the approval process. His advice? Tell reviewers what they want to hear in the manner they want to hear it. Sounds simple, right?
Find out more at this special event designed for angel investors, startup companies with medical devices or drug candidates, entrepreneurs, and others engaged in the life sciences ecosystem. There will be ample time for Q&A!