The Directorate General of Drug Administration (DGDA) under the Ministry of Health & Family Welfare, Government of the People's Republic of Bangladesh, is the Drug Regulatory Authority of the country. This DGDA supervises and implements all prevailing Drug Regulations in the country and regulates all activities related to import, procurement of raw and packing materials, production and import of finished drugs, export, sales, pricing, etc. of all kinds of medicines including those of Ayurvedic, Unani, Herbal and Homoeopathic systems.drugs and medicines. At present, there are 47 district offices under the DGDA in the country. All the officers of the DGDA function as "Drug Inspector" in pursuant to the Drug Laws and assist the Licensing Authority to discharging his responsibilities properly. Besides, a number of Committees, such as Drug Control Committee (DCC), Standing Committee for imports of raw materials and finished drugs, Pricing Committee and a number of other relevant Committees, which comprise of experts of different fields, are there to advice Licensing Authority and recommend him about the matters related to drugs and medicines.
DGDA Office Locations
DGDA Notice Board
- EOI for SELECTION OF A FIRM FOR DEVELOPINGONLINE REPORTING SYSTEM OF Fake medicine, overpricing of medicine & adverse drug reaction (ADR)
- Paracetamol 500 mg + DL-Methionine 100 Tablet, Pioglitazone 30 mg & 45 mg Tablet and Rosiglitazone 2 mg & 4 mg Tablet Registration Cancelled
- New Member Inclusion in the Drug Control Committee