Ministry of Public Health - Service Details

Registration of Manufacturer of Pharmaceutical Products.

Target Audience

Pharmaceutical Companies

Pharmaceutical factories for pharmaceuticals

Pharmaceutical Manufacturers

Related Department/Corporation

Pharmacy and Drug Control Department - Registration & Drug Pricing

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.

Service Details

Registration of Manufacturer of Pharmaceutical Products.

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