As a Technical Regulatory Officer
Manage Common Technical Document/electronic Common Technical Document application project in October Pharma & monitor applications under regulatory review.
Identifying regional regulatory requirements of different Ministry Of Health in different countries.
Ensure the compliance to regulatory filings.
Participate & share actively in identification of new products documents from regulatory point of view.
Interact & communicate with outside experts, research & development centers for issues related to product development for bioequivalence studies and Expert reports.
Interact & communicate with API "active pharmaceutical ingredients" vendo...