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    Eric Bannon

    Medical Device Consultant Specializing in Regulatory and Clinical Affairs

    Eric Bannon is a dynamic executive with extensive global experience in implementing creative regulatory and clinical strategies across various therapeutic areas. He is known for his hands-on approach and building high-performance teams to drive company growth. With a track record of successfully developing and leading complex plans, Eric is a results-driven manager with a knack for adapting to changes in plan execution. His expertise includes global regulatory strategy, US submissions, early-stage start-ups, and clinical initiative implementation.

    Throughout his career, Eric has achieved milestones in regulatory affairs, such as leading the approval of multiple IDEs, securing early CE Mark approvals, and navigating worldwide approvals for clinical trials. He has also played a key role in over 40 successful 510(k) submissions for market launches. In the realm of clinical strategy, Eric has built teams for large patient trials, completed first-in-human trials, and integrated reimbursement measures for trial costs coverage.

    Having studied Microbiology at the University of Maine and Massachusetts Institute of Technology, Eric Bannon brings a strong educational background to his professional endeavors. His career includes notable roles such as Vice President of Clinical and Regulatory Affairs at AlvaMed, Inc., and various leadership positions in regulatory and clinical affairs at companies like Fractyl Laboratories Inc., NDO Surgical, and Cortek.

    Eric Bannon
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    Location

    United States