Strong with Regulatory documentation
MFR/SOP/AMV(analytical Method Varidation),ACTD/CTD, Dossier Preparation
Having a sound knowledge of COPP preparation, application filing and grant
Will be responsible for handling Regulatory affairs Documentary requirements.
He should have sound knowledge and experience in ROW Markets, African Countries and South East Asia.
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Legal , Regulatory , Intellectual Property
Role Category:Drug Regulatory Affairs/Documentation
Role:Regulatory Affairs Manager
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