Application Process and Requirements for Post-Approval Changes of Biological Products Adopting the World Health Organization Guidelines for Changes to Approved Vaccines and Biotherapeutic Products for Human Use; (91 page(s), in English)

Draft Decree promulgating the lists of chemicals subject to management under the Law on Chemicals No. 69/2025/QH15; (65 page(s), in Vietnamese)

Prescribing the Guidelines for the Application of Certificate of Good Manufacturing Practice (GMP) Compliance for Local and Foreign Pharmaceutical Manufacturers; (49 page(s), in English)