To prepare documents Technology Transfer Document, Product scale up report, Product development report, Chemistry manufacturing & control, Polymorphism study etc.
To collect necessary information from all concerned Department.
To prepare DMF (Drug Master File) for Regulatory Market.
To ensure that manufacturing procedure and specification of materials are in accordance with the submitted DMF.
To solve query related to Regulatory market & various customers related to Drug Master File.

Keyskills: Regulatory Affairs Drug Regulatory Affairs Dossier Preparation Dmf