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Helen Johnson

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Last update: 20.10.2020

Regulatory affair consultant for medical device

Graduation: not provided
Hourly-/Daily rates: show
Languages: English (Native or Bilingual)

Keywords

Skills

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.

Project history

Local Availability

Only available in these countries: USA
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