Ceo/Consultant
SG Consulting-Pro Ltd.
Sharon Goldfarb (BSc Life Sciences Tel Aviv University, partial studies toward a Master in Regulatory Affairs SDSU) has been working in the medical device fields of regulatory affairs, clinical trials, quality assurance and marketing since the turn of the century. With 22 years of experience, Sharon has worked with medical devices from several different disciplines of medicine helping various companies build and implement regulatory and clinical strategies and marketing submissions, studies from the pre-clinical phase through the full blown clinical investigations and subsequent regulatory processes. Sharon has successfully implemented and managed several international studies for medical devices, which led to successful regulatory marketing submissions. In addition to work on regulatory and clinical management, she provides aid in medical writing, Clinical Evaluation Plans and Reports for medical device submission to the EU as well as Post Market Clinical Follow-up and other US and EU regulatory, clinical and quality documentation
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Tuesday, September 13, 2022
1:30 PM – 2:00 PM MST