Ministry of Health issues new and renews more than 500 drugs and pharmaceuticals

The Drug Administration of Vietnam, Ministry of Health informed that among more than 500 drugs and generic drugs newly granted and having their circulation registration numbers extended this time, there are 414 domestically produced drugs and 68 generic drugs...

500 original drugs, medicines... have just had their registration numbers renewed and renewed by the Ministry of Health .

Previously, in March and early April 2024, the Ministry of Health had new issuances, extensions and announcements of thousands of domestically produced drugs, generic drugs and drugs and pharmaceutical ingredients implementing Resolution 80 of the National Assembly (12th extension announcement).

It is known that the original pharmaceutical products and brand-name drugs that have been newly granted circulation registration numbers and have had their registration numbers extended in recent times are quite diverse in terms of pharmacological effects, including drugs for treating cancer, cardiovascular diseases, hypertension, diabetes, antiviral drugs, drugs for treating respiratory diseases, antibiotics, antipyretics, pain relievers, other common anti-inflammatory drugs... and vaccines and biological products that are in high demand for use in medical examination and treatment, and disease prevention.

The Ministry of Health requires that drug manufacturing and registration establishments are responsible for producing drugs in accordance with the records and documents registered with the Ministry of Health and must print the registration number issued by the Vietnamese Ministry of Health on the drug label...

The Ministry of Health also requires drug manufacturing and registration facilities to coordinate with treatment facilities to comply with current regulations on prescription drugs, monitor the safety, effectiveness, and adverse effects of drugs on Vietnamese people, and synthesize and report according to regulations.

The drug registration facility must ensure that it maintains its operating conditions during the validity period of the drug and drug ingredient registration certificate. In case it no longer meets the operating conditions, the registration facility must be responsible for changing the registration facility according to regulations.

Drug manufacturing facilities must ensure the operating conditions of the manufacturing facility during the validity period of the drug and drug ingredient circulation registration certificate.

Source: https://www.baogiaothong.vn/bo-y-te-cap-moi-gia-han-hon-500-thuoc-biet-duoc-192240513105520481.htm