10/20/2020 updated

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Regulatory affair consultant for medical device

USA
USA
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

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