According to the Drug Administration, facilities must strictly control input materials, production processes, storage and distribution of drugs, while preventing the risk of cross-contamination and product confusion.
Units are required to review production processes and testing records to ensure compliance with approved registration records.
The Ministry of Health also requested local Health Departments to strengthen inspection and supervision of GMP compliance, especially at facilities that simultaneously produce drugs and health protection foods, to ensure quality and safety for users.
Source: https://nhandan.vn/ video -Ministry of Health requires strengthening of GMP-regulations in medicine production-post884578.html
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