THAILAND: Thai FDA Introduces an Expedited Registration Route for IVD Medical Devices with Prior WHO Approval – March/April 2023

• 2023-03-27 08:27:31

Thai FDA announces 'Thailand FDA - WHO Collaborative Registration Procedure (CRP) for in vitro diagnostics (IVDs)', an expedited medical device registration program aimed at reducing the time required for manufacturers and importers to register their products. The program officially commenced on December 28, 2022, onward.

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HONG KONG: Changes in Trial Schemes and Continuation of the Expedited Approval Schemes for Class II, III, and IV General Medical Devices – February 2022

• 2022-02-18 08:16:14

Hong Kong's MDD has announced a few changes in the trial schemes on the acceptance of some reference agencies approval. MDD also announced the regularization of the expedited approval scheme for Class II/III/IV General Medical Devices.

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HONG KONG: Trial Scheme for Expedited Approval of Class II/III/IV General Medical Device Listing Applications Will Close by The End of 2021 – December, 2021

• 2021-12-27 05:12:19

MDD announced the closing of the ongoing trial scheme for expedited approval of Class II/III/IV General Medical Device Listing Application on 31 December 2021. The limit application for applicants who wish to apply through the trial scheme have been lifted.

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