Assist in preparing and compiling regulatory dossiers for product registration, variation, and renewals (under guidance).

Support the submission process to national and international regulatory authorities (e.g., CDSCO, US FDA, EMA, etc.).

Help maintain up-to-date regulatory files and databases.

Assist in reviewing product labels, leaflets, and promotional materials for compliance.

Learn and stay informed about current pharmaceutical regulations and guidelines.

Coordinate with departments such as Quality Assurance, R&D, Production, and Marketing for document collection and support.

Help respond to queries from regulatory agencies with appropriate documentation (under supervision).

Participate in training programs and internal meetings related to regulatory affairs.