Decision 166/QD-BYT: On the issuance of criteria and principles for evaluating the common submission dossier template (CSDT) for medical devices in accordance with ASEAN regulations, applicable to medical devices other than in vitro diagnostic medical devices

Decision 166/QD-BYT: Issuing the “Criteria, Principles for Evaluating the Common Submission Dossier Template (CSDT) for...

Regulations on advertising for Health Supplement

Advertising is a crucial activity for businesses aiming to increase awareness and positive impressions of...

Health Supplement Production Conditions 

The production of health supplements is a process that requires strict adherence to regulations on...

Strict regulation of health supplement advertisements

Taking strict measures against social media platforms, permanently deleting domains upon the discovery of violations...

GMP of Health Supplement

Health supplements are becoming increasingly integral to dietary regimes, aiding in improving health and preventing...

Learn medical device registration from a-z at Medgate

Are you looking to transition into the field of medical device registration but lack basic...

Conditions, Procedures, and Documentation for Opening a Medical Device Business Store

Opening a business store selling medical devices requires compliance with legal regulations, as medical devices...

Business conditions for the inspection and calibration services  of medical devices

Legal Basis Decree No. 98/2021/NĐ-CP issued on November 8, 2021: Management of medical devices. Decree...

ISO 13485- Medical Devices Quality Management System

What is ISO 13485? ISO 13485 is an international standard developed by the International Organization...

Import cosmetic declaration service

Imported Cosmetic Declaration Cosmetics intending to circulate in the market must be issued a Cosmetic...