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- 1 Circular No. 9/2020/TT-BYT dated June 10, 2020 on amendments to the Circular No. 03/2018/TT-BYT on good distribution practices for pharmaceutical products and pharmaceutical starting materials
- 2 Circular No. 36/2018/TT-BYT dated November 22, 2018 on Good Storage Practices for medicinal products and medicinal materials
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- 1 Circular No. 48/2011/TT-BYT of December 21, 2011, promulgating principles of good distribution practice
- 2 Circular No. 36/2018/TT-BYT dated November 22, 2018 on Good Storage Practices for medicinal products and medicinal materials
- 3 Circular No. 9/2020/TT-BYT dated June 10, 2020 on amendments to the Circular No. 03/2018/TT-BYT on good distribution practices for pharmaceutical products and pharmaceutical starting materials
- 4 Circular No. 9/2020/TT-BYT dated June 10, 2020 on amendments to the Circular No. 03/2018/TT-BYT on good distribution practices for pharmaceutical products and pharmaceutical starting materials
- 1 Circular No. 11/2018/TT-BYT dated May 4, 2018 on Drug/Drug Ingredient Quality
- 2 Decree No. 75/2017/ND-CP dated June 20, 2017, defining functions, tasks, powers and organizational structure of Ministry of Health
- 3 Decree No. 54/2017/ND-CP dated May 08, 2017, guidelines for implementation of the Law on Pharmacy
- 4 Law No. 105/2016/QH13 dated April 06th, 2016, on pharmacy
- 1 Circular No. 11/2018/TT-BYT dated May 4, 2018 on Drug/Drug Ingredient Quality
- 2 Decision No. 47/2007/QD-BYT of December 24, 2007, on the application of good manufacturing practice principles and standards, good laboratory practice principles, good storage practice principles and good distribution practice principles to establishments that manufacture, test, trade in, distribute, import, export, stockpile and store vaccines and medical biologicals.