Sharon Sax - Clinical & Regulatory Consultant
medical devices
About
Bringing medical devices from R&D into the clinical environment – drafting a clinical-regulatory strategy, designing the study protocol, establishing the required internal and external infrastructure to support the clinical activity, managing the clinical study according to GCP and MDR.
Keywords
clinical trials
feasibility studies
transition from rd to clinical
medical equipment manufacturing
health care
health
wellness & fitness
hospital & health care
medical devices
Company Information
-
Employees 1
