RAQA Intern

• Basic understanding of the regulatory requirements under Medical Device Rules, 2017 and the Drugs & Cosmetics Act.

• Assist in preparing and organizing regulatory documentation and submissions for new products and retentions.

• Support RA team in remediation activity for existing submissions / approvals

• Maintain and update regulatory databases, trackers, and filing systems.

• Conduct research on regulatory guidelines and updates issued by authorities.

• Track regulatory timelines and maintain submission status reports.

• Coordinate with internal teams to gather information required for regulatory

• Support the Regulatory Affairs team with administrative and documentation tasks.

• Understand the complaint and adverse event reporting requirements and report such events to the competent authority within the stipulated timelines.

Understand the BIS registration process and requirements