Profile Summary
Nanna F.
Senior Regulatory Affairs Specialist in LatAm, specializing in Mexican and Peruvian medical device regulation. Medical writer with experience ...
Smita S.
Extensive and Diversified experience in Audits and Compliance, Quality management systems, Process excellence, Training and Coaching. Working ...
Ranjith P.
• Prepare Technical documentation for Medical Device CE marking • Support MDR Compliance execution by reviewing/updating/creating Technical doc...
Bicky M.
With over 15 years of experience in clinical research in different positions, including CRA, Regional Study Manager, Local Study Manager, Study...
Abdullah B.
Having diverse knowledge and experience on legal and religious issue of medical/medicinal cannabis use and authorisation. Content writing. Me...
Sreejith K.
17 years with multiple consulting gigs across North America and Germany. Completed over 100 Projects.Business mind with Project Management,Risk...
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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