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GMP International



medical products


It is carried out according to appendix 1 to the Resolution of the Cabinet of Ministers of the Republic of Uzbekistan from September 18, 2019 of No.788

1. Documents of the production area (Site Master File)

2. List of documents standard operating procedure (SOPs)

3. List of processes of quality management system (SMK)


1. Recognition of the decision of the working body to issue a certificate as illegal;

2. When it is established that the certificate was obtained using forged documents and information;

3. During the validity period of the certificate, changes are made that affect the requirements of Good Practice (GxP) and the applicant does not apply to the working body for verification.

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