• 2023-10-20 06:31:20

Recently, TFDA has announced an amendment to the classifications of medical devices. The scopes and identifications of several medical device classifications have been updated to provide more specific and clearer instructions. Among these, the risk level of 3 classifications has been re-determined and there are 11 new additional classifications.

• 2023-08-23 06:09:04

Due to Regulation (EU) 2023/607, the transition period is extended. Some timelines of the related factsheet or guidance are modified accordingly.

• 2023-01-19 05:49:15

It is announced that the MDA amended the terms of the establishment license granted under section 15 of Act 737 in accordance with Act 20's provisions. At least 90 days before the license expires, the establishments must submit an application to the Authority for a renewal.

• 2022-12-27 07:40:22

Indonesia Halal Assurance Agency have issued Decree of Head of BPJPH Regulation Number 133 of 2022 concerning Procedures for Requesting Data Amendment on Halal Certificates. This regulation outlines the types of amendment allowed and the procedures for amendment application in Halal certificates.

• 2022-12-27 03:31:34

An official letter number 6698/BYT-TB-CT was released on November 21, 2022, by the Vietnam Ministry of Health, collecting comments for a draft decree amendment of decree 98/2021/ND-CP

• 2022-02-18 09:44:59

On 9 December 2021, the Vietnamese government issued Decree No. 111/2021/ND-CP amending and supplementing a number of articles of Decree No. 43/2017/ND-CP on Goods Labels, including medical devices ("Decree 111"), which will take effect as of 15 February 2022.

• 2021-04-26 02:39:59

Australia Department of Health (DoH) Therapeutic Goods Administration (TGA) has made some amendments and issued the Therapeutic Goods Amendments (2020 Measures No. 2) Act 2021, focusing on unique device identification (UDI) under Therapeutic Goods Act 1989.

• 2020-08-11 05:46:22

PFDA adjusted some transactions that usually requires face to face interactions. However, PFDA reminded that post-marketing surveillance activities for all medical devices will be continue.

• 2020-03-16 07:03:45

Ministry of Public Health Announcement regarding Amendment of the Application Form in accordance with the Ministerial Regulations, Specify the Rules, Procedures and Conditions for Registration of Establishment Import License 2019 (No.3) and Registration of Establishment Manufacturing License 2019.

• 2020-03-16 06:50:01

Medical Devices (Amendment) Rules, 2020 has been newly issued to amend the Medical Devices Rules, 2017. Medical Devices (Amendment) Rules, 2020 will be effective 1st April 2020. All medical devices in India is now to be regulated as “drugs”.