Regulatory Compliance
Prepare license applications for recent pharmaceutical products.
Renew existing manufacturing, marketing, and distribution licenses.
Compile technical documentation for product registration dossiers.
Submit accurate data packages to health authorities.
Liaison & Communication
Coordinate with government drug regulatory bodies directly.
Respond to official technical queries and audit findings.
Advise internal manufacturing teams on compliance standards.
Track changes in local and international pharmaceutical laws.
Documentation & Quality
Maintain a secure archive of all valid licenses.
Review product labels, packaging, and inserts for legal compliance.
Verify Certificate of Pharmaceutical Product (COPP) documents.
Support internal audits to prepare for official inspections.