Rachel Weissbrod

VP Clinical, Regulatory & QA Affairs at Medasense

Ms. Weissbrod brings twenty years of experience in the medical device industry in clinical strategy and market development, regulatory affairs and quality assurance, product innovation and management. Prior to joining Medasense, Ms. Weissbrod was a Global Director of Medical Affairs & Value Based Healthcare at Medtronic focusing on clinical market development for patient monitoring devices.

Ms. Weissbrod has held leadership roles in Quality Assurance, Regulatory & Clinical Affairs at Covidien, Oridion Medical and additional start-up companies with extensive experience in leading teams in the development and execution of global regulatory, quality and clinical strategies supporting new product development and commercialization.

Ms. Weissbrod holds a B.Pharm, and an MBA, both from the Hebrew University, Jerusalem, Israel.


Timeline

  • VP Clinical, Regulatory & QA Affairs

    Current role