Pharmaceutical Companies
Pharmaceutical factories for pharmaceuticals
Pharmaceutical Manufacturers
Service provided by Registration & Drug Pricing Section of Pharmacy & Drug Control department, through which pharmaceutical products Manufacturer registration is approved, if the required conditions are met
Requirements
- Legalized and valid Good Manufacturing Practice (GMP) certificate from the health authority in the country of origin.
- Legalized and valid Manufacturing License (ML) from the health authority in the country of origin.
- Legalized relationship letter between the marketing authorization holder (MAH) company and the manufacturer.
- List of the products manufactured by the manufacturer showing their pharmacological group, Generic name & trade name.
- Soft copy of the Site master file (according to WHO format).
- Registration certificate of the manufacturing site in gulf countries and other countries (if available).
Note: Legalized means authentication of the document from embassy of Qatar in country of origin.
Registration Procedure
- Submission of the application via the electronic system PDCD E-system (E-Service link below).
- Assessment of the application and notification of the Agent of any further requirements if needed.
- Presenting the file to registration committee and inform the Agent with the committee decision.
- In case of approval a printable certificate is autogenerated from the E-System.