Digital

1. Letter specifying the requested changes.

2. Good Manufacturing Practice (GMP) certificate for the factory.

3. Manufacturing License (ML) for the factory, issued by the health authorities in the country of origin.

1. The applicant must have an account on the Pharmacy e-System.

2. A registered agent must exist.

3. A registered marketing company must exist.

4. A registered factory must exist.

Free

pdcdsupport@moph.gov.qa / Tel No: +974 44070900

3 hours and 20 minutes