To prepare and compile dossiers for allotted countries (ROW) in CTD format (Countries worked on Anglo African countries, French West African countries)
Arrangement of samples
Application and review of legal documents for Pharmaceutical Product.
Routine update of regulatory status.
Overview
Industry -
PHARMACEUTICAL / MEDICAL DEVICES / CRO, Pharmaceutical - Formulations
Functional Area -
Regulatory Affairs / Corporate Affairs
Job Role -
Officer / Executive - Regulatory Affairs