Circular No. 32/2018/TT-BYT
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- Vietnam: 04 criteria for exemption of stages of clinical trial of drugs before marketing authorization
- 09:44, 21/03/2019
- The Ministry of Health of Vietnam issued Circular No. 32/2018/TT-BYT on marketing authorization of drugs and medicinal ingredients.
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- Vietnam’s Circular 32: Guidelines for procedures for granting marketing authorization of drugs
- 09:32, 16/11/2018
- Recently, the Ministry of Health of Vietnam issued Circular No. 32/2018/TT-BYT on marketing authorization of drugs and medicinal ingredients.
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- Vietnam: Cases eligible for quick validation of applications for import of drugs without marketing authorization
- 09:09, 16/11/2018
- This is a content specified in Circular No. 32/2018/TT-BYT of the Ministry of Health of Vietnam on marketing authorization of drugs and medicinal ingredients.
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- Vietnam: Guidelines for procedures for renewal of applications for the marketing authorization of drug from September 01, 2019
- 09:23, 15/11/2018
- This is a notable content specified in Circular No. 32/2018/TT-BYT of the Ministry of Health of Vietnam on marketing authorization of drugs and medicinal ingredients.
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- Circular 32: Vietnam’s regulations on reporting monitoring carried out by pharmaceutical-trading establishments
- 08:57, 15/11/2018
- This is a notable content specified in Circular No. 32/2018/TT-BYT of the Ministry of Health of Vietnam on marketing authorization of drugs and medicinal ingredients.
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- Vietnam: Manufacturers of drugs may change the authorization holder within 30 days
- 08:39, 15/11/2018
- This is one of the responsibilities of manufacturers of drugs/medicinal ingredients specified in Circular No. 32/2018/TT-BYT of the Ministry of Health of Vietnam on marketing authorization of drugs and medicinal ingredients.
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- Vietnam: 04 cases of exemption of one or some stages of clinical trial of new modern drugs, vaccines, biologicals before marketing authorization
- 08:32, 15/11/2018
- Recently, the Ministry of Health of Vietnam issued Circular No. 32/2018/TT-BYT on marketing authorization of drugs and medicinal ingredients.
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