Circular No. 35/2018/TT-BYT
-
- Vietnam: Documents used as basis for inspection of GMP compliance by a pharmacy business establishment are those included in its application for certificate of eligibility for pharmacy business
- 09:00, 10/01/2019
- This is a notable content of the Circular No. 35/2018/TT-BYT of the Ministry of Health of Vietnam on Good Manufacturing Practices (GMP) for pharmaceutical products and pharmaceutical starting materials.
-
- Vietnam: Where to submit the application for recognition of GMP compliance?
- 08:59, 04/01/2019
- On November 22, 2018, the Ministry of Health of Vietnam issued Circular No. 35/2018/TT-BYT on Good Manufacturing Practices (GMP) for pharmaceutical products and pharmaceutical starting materials.
-
- Vietnam: 08 changes that the manufacturer shall apply for the certificate of eligibility for pharmacy business
- 08:57, 04/01/2019
- The Ministry of Health of Vietnam issued Circular No. 35/2018/TT-BYT on Good Manufacturing Practices (GMP) for pharmaceutical products and pharmaceutical starting materials.
-
- 06 steps for inspection of GMP compliance in Vietnam
- 08:55, 04/01/2019
- The Ministry of Health of Vietnam issued Circular No. 35/2018/TT-BYT on Good Manufacturing Practices (GMP) for pharmaceutical products and pharmaceutical starting materials.
-
- Vietnam: 07 cases of surprise inspection of GMP compliance at the manufacturer
- 08:54, 04/01/2019
- The Ministry of Health of Vietnam issued Circular No. 35/2018/TT-BYT on Good Manufacturing Practices (GMP) for pharmaceutical products and pharmaceutical starting materials, amending Circular No. 04/2018/TT-BYT.
Most view
SEARCH ARTICLE
