1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Prepare and submit regulatory dossiers for product registrations, renewals, import licenses, and approvals.
Coordinate with regulatory authorities such as Central Drugs Standard Control Organization (CDSCO).
Manage regulatory compliance across India, Sri Lanka, Bangladesh, and Pakistan.
Support clinical trial application submissions, amendments, and approvals.
Obtain import/test licenses for clinical trial products.
Work closely with clinical, supply ...