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VIETNAM: MINISTRY OF HEALTH EXTENDED THE VALIDITY OF IMPORT LICENSE BY AMENDING AND SUPPLEMENTING DECREE NO. 98/2021/ND-CP, AS REVISED BY DECREE NO. 07/2023/ND-CP – February/March 2025

VIETNAM: MINISTRY OF HEALTH EXTENDED THE VALIDITY OF IMPORT LICENSE BY AMENDING AND SUPPLEMENTING DECREE NO. 98/2021/ND-CP, AS REVISED BY DECREE NO. 07/2023/ND-CP – February/March 2025

  • 2025-02-20 10:09:30

Decree No. 04/2025/NĐ-CP, released on January 1st, 2025, by Vietnam MOH, extending the validity of import license until June 30, 2025, on the Decree amending and supplementing of Clause 2, Clause 3, and Clause 4, Article 76 of Decree No. 98/2021/ND-CP, as revised by Decree No. 07/2023/ND-CP, regarding medical device management.

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THAILAND: Food and Drug Administration Announcement Regarding the Document Preparation for Licensed Medical Device Manufacturing / Import License Renewal and Notified Medical Device Manufacturing / Import License Renewal – October, 2020

THAILAND: Food and Drug Administration Announcement Regarding the Document Preparation for Licensed Medical Device Manufacturing / Import License Renewal and Notified Medical Device Manufacturing / Import License Renewal – October, 2020

  • 2020-10-19 09:48:24

Food and Drug Administration has announced sets of documentation required for Licensed Medical Device Manufacturing / Import License Renewal and Notified Medical Device Manufacturing / Import License Renewal that will expire in December 31st, 2020.

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THAILAND: Thai FDA announce that manufacturer and importer must proceed medical device to be licensed registration 2020 – June, 2020

THAILAND: Thai FDA announce that manufacturer and importer must proceed medical device to be licensed registration 2020 – June, 2020

  • 0000-00-00 00:00:00

Despite the effect of COVID-19 outbreak, ThaiFDA continued to perform at its best for the Medical device regulation reform update. Future regulation follows Risk- based Classification, while current regulation follows Policy- based Classification. Thai FDA Announced that Manufacturer and Importer must Proceed Medical Device to be Licensed Registration.

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