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Regulation, Clinical and Software for Medical Devices

BIG SAVINGS END IN:

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November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, Minnesota

Rina Sant
Associate Director, Post-Market Clinical Oversight at Abbott
Speaker

Profile

A Medical Doctor (M.D.) with a Master of Science (MS) in Applied Clinical Research. A Medical Research Professional with 13 years of experience in the global medical device life cycle from conception through marketing in clinical research, including consulting on EU MDR. Specialized medical and clinical research expertise in the Cardiovascular therapeutic area.

Agenda Sessions

  • Proactive PMS and Maneuverable PMCF Needs in Continuous PMCF world:

    11:10am
  • Getting Real with Data: Collecting and Using Real-World Evidence (RWE)

    1:45pm
  • Ask the Experts: Medical Devices

    4:40pm