Product Registration & Authorisation
Implementing effective regulatory strategies for human and veterinary medical products, medical devices and cosmetics.
Overview
 The Department of Product Evaluation and Registration (DPER) plays a pivotal role in achieving the strategic objective of streamlining registration processes. This department focuses on implementing effective regulatory strategies for human and veterinary medical products, medical devices and cosmetics
Scope:
- Human medicines- including complementary medicines ​
- Veterinary medicines​
- Medicals Devices​
- Cosmetics department
Responsibilities
Human Medicines, Including Complementary Medicines
Evaluation and registration of pharmaceutical and complementary products intended for human use, ensuring they meet regulatory standards and are safe for consumption.
Veterinary Medicines
Assessment and registration of veterinary products to safeguard animal health and ensure compliance with both local and international regulations.
Medical Devices
Regulation of medical devices, including their evaluation, registration, and monitoring to ensure they are safe, effective, and of high quality.
Cosmetics
Oversight of cosmetic products through notification and compliance checks to ensure they meet safety standards for public use.