Finished medicine

Import registration requirements:

1. Letter of Authorization from the manufacturer (proof of authorization).

2. Form DA 2/88 – This DGDA-prescribed form is required for the introduction of a first-time molecule in Bangladesh.

3. COPP of Manufacturing country – attested by Bangladesh Embassy in that country.

4. COPP from any one of the following countries: USA, UK, Japan, Australia, Switzerland, France, Germany (Bangladesh Embassy attested, Original).

5. Product profile (CTDA, module-2 only)

6. Company profile – pdf

7. Packaging Materials (empty): Box, Label, Direction slip, Labeling must reflect the Brand name, Manufacturer name, Country of Origin, Mfg. date, Expiry date & Lot no.

8. FDA or, EMA, or, UKMHRA approval reference

*Govt. treasury fee: USD 600/product

For Veterinary medicine:

COPP from any one of the following countries: 

Australia, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Hungary, Ireland, Italy, Japan, Netherlands, Norway, Singapore, Sweden, Switzerland, UK, USA, Russia, Poland, Spain, South Korea, Czechoslovakia (Original copy)