Sound knowledge of compiling registration dossier , Reviewing & filling of dossier of E-CTD Projects for Europe , US & ROW market for solid oral dosage, Parenteral preparations and sterile dosage form etc.
Min 10 to 15 yrs for Regulatory ( EU , US & ROW Market)
Must have deal USFDA, WHO/ European Regulatory Bodies.
Exp. of filing DMFs for approval in US/ Europe
Willing to work in Ahmedabad region