LABELING REQUIREMENTS FOR MEDICAL DEVICES

Medical device labeling is not only a means of product identification but also a legal...

REQUIREMENTS FOR PRODUCT TESTING OF HEALTH SUPPLEMENTS

Product testing is a mandatory step to ensure food safety and protect consumer rights prior...

CHANGES THAT REQUIRE RE-REGISTRATION OF HEALTH SUPPLEMENT PRODUCT ANNOUNCEMENT

To legally circulate health supplements (HS) in the Vietnamese market, businesses are required to register...

What is the Certificate of Free Sale for Health Supplements? Required Documentation and Procedures for obtaining a CFS?

What is the Certificate of Free Sale (CFS) for Health Supplements? The Certificate of Free...

Intructions for Searching Registration Number of Medical Devices

To be legally marketed, a medical device must be issued a registration number by Vietnam’s...

Template for medical device import license

Applying for an import license of medical devices The medical devices lacking a circulation number...

Regulations on importing medical devices

Currently, the state encourages domestic enterprises to produce medical devices for export. However, the increasing...

The Importance of Medical Equipment Quality Inspection

In the field of healthcare, medical equipment plays an essential role, not only supporting doctors...

Legal Consequences of Using Unregistered Medical Equipment

Medical equipment plays an important role in supporting modern medicine. They are not only effective...

Enterprises without circulation registration numbers will not be able to import class C, D medical devices from 2025.

According to the provisions of Decree 07/2023/ND-CP, Section 18 of the amendment and supplement to...