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Regulatory Affairs Professional
I'm a clinical regulatory affairs professional with experience in taking medical device products to market in different countries. My experience includes all phases, including study design, budgeting and timeline development, medical writing (e.g., clinical protocol, IND, IDE, etc), clinical study initiation and oversight, data management, premarket notifications (e.g., 510(k), BLA, etc), clinical study reports, and direct interaction with regulatory agencies.
Clinical Regulatory Affairs
About Me
Industry: |
Science & Biotech |
|---|---|
Occupation: |
Clinical Regulatory Affairs |
Education level: |
Master |
Will Relocate: |
Yes |
