A. Drug Evaluation Section (DES)
1.Registration of Medicinal Products
2. Renewal of registration of medicinal products
3. Post Approval Variation Application (PAVA) of medicinal products
4. Product registration transfer of medicinal products
5. Listing certificate for Health and Feed Supplement
6. Import Authorization for Medicinal Products
7. Issuance of Export Authorization
8. Issuance of Free Sale Certificate (FSC)
8. Issuance of Certificate of Pharmaceutical Products (CoPP)
9. Issuance of Clinical Trial Authorization
B. Licensing and Vigilance Section (LVS):
1. Clearance and control of medical products related advertisement
2. Disposal of Medical product wastes
3. Issuance of Provisional Authorization for Manufacture (PAM) of medicinal products
4. Issuance of technical authorization for manufacture (TAM) of medicinal products
5. Post-Approval Variation and Renewal of technical authorization for manufacture
6. Registration/Renewal of Professional as Competent Person
7. Issuance of GMP certificates
8. Technical authorization/renewal for sale & distribution of medicinal products
9. Change of ownership of technical authorization, location of pharmacy, name of pharmacy and change in competent person
10. Lot Release of Vaccine
C. Medical Device Section (MDS):
1. Registration of Medical Devices
2. Renewal of Medical Device registration
3. Post Approval Variation Application (PAVA) of Medical Devices
4. Import Authorization for Medical Devices