In Bangladesh, any business involved in selling, storing, distributing, or manufacturing medicines must obtain a valid Drug License issued by the Directorate General of Drug Administration (DGDA) under the Ministry of Health and Family Welfare. This is governed by the Drugs Act, 1940 and the Drugs (Control) Ordinance, 1982.
Operating without a valid license is a punishable offense under Bangladeshi law, resulting in heavy fines, business closure, or imprisonment.
Drug licenses are issued across multiple categories—including retail pharmacy, wholesale, manufacturing, and import/export — each with its own requirements regarding qualified pharmacists, proper storage facilities, and compliance with Good Storage or Manufacturing Practices (GSP/GMP).
The process involves document preparation, DGDA submission, and a mandatory site inspection before approval is granted. At Segunbagicha Consultancy, we simplify this entire process for you — ensuring your business is legally compliant, professionally prepared, and ready for DGDA approval without hassle.