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Product, article supervision

Approval and Issuance of Certificate of “Good Manufacturing Practice for Pharmaceutical Products (GMP)”

Service Introduction

Procedures for the issuance of certificate of Good Manufacturing Practice for Pharmaceutical Products (GMP) to eligible pharmaceutical manufacturing plants.

Service target and eligibility

Individuals/ legal persons holding the “Licence for Pharmaceutical Production” issued by the Pharmaceutical Administration Bureau.

Result of application

The Pharmaceutical Administration Bureau will issue a certificate of Good Manufacturing Practice for Pharmaceutical Products (GMP) to the pharmaceutical manufacturing plants that meet the requirements.


Executive department and unit: Pharmaceutical Administration Bureau-Inspection and Licensing Department- Licensing Division

Correspondence address: Avenida Sidónio Pais, n.º 51, Edif. “China Plaza”, 4.º andar, Macau

Telephone:(853) 8598 3522

Facsimile:(853) 2852 4016

Content provider: Pharmaceutical Administration Bureau (ISAF)

Last modified: 2022-01-01 02:01

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All information on this site is based on the official language of the Macao Special Administrative Region. The English version is the translation from the Chinese originals and is provided for reference only. If you find that some of the contents do not have an English version, please refer to the Traditional Chinese or Portuguese versions.