10/20/2020 updated


100 % available
Regulatory affair consultant for medical device
USA
USA
BiopharmaceuticalsClinical TrialsComplianceDrug DiscoveryQuality ManagementRisk AnalysisMedical MaterialRegulatory Affairs
Experienced Quality Assurance Consultant with a demonstrated history of working in Medical devices, Drugs, Biologics, and Combination products. Skilled in Regulatory Affairs, Quality Assurance, Clinical trials, New Drug Application (NDA), Investigational Drug Application (IND), Risk Assessment, Biologic License Application (BLA), and Consulting.
Languages
EnglishNative speaker