November 2022

Admin folder for amendments

Malaysia: MDA Issued Fourth Edition Guidance Document “Change Notification for Registered Medical Device” (MDA/GD/0020)

On November 21, 2022, the MDA has announced the release of the Fourth Edition Guidance Document “Change Notification for Registered Medical Device” (MDA/GD/0020). This guidance document is a revision from the Third Edition that was issued in November 2018, to provide the medical device industry a guidance on the categories of changes, the principles of […]

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Barcode labels on rolls

MDA Issued Sixth Edition Guidance Document “Requirements for Labelling of Medical Devices” (MDA/GD/0026)

On November 21, 2022, the MDA has announced the release of the Sixth Edition Guidance Document “Requirements for Labelling of Medical Devices” (MDA/GD/0026). This guidance document provides minor updates from the Fifth Edition that was issued on 14 June 2022. This document provides guidance to the manufacturers and authorized representatives on the content of medical

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Clinical trial injection bottle and hypodermic needle

Singapore: GN-20: Guidance on Clinical Evaluation Revision 2

The Health Sciences Authority (HSA) Singapore published minor update of guidance document entitled GN-20 R2 Guidance on Clinical Evaluation on 01 November 2022, stipulating clinical investigations carried out by or on behalf of product owner are encouraged and expected to be designed, conducted, and reported in accordance with international ISO 14155 – Clinical Investigation of Medical Devices for

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A shelf of manilla files

Thailand: Notification of the Ministry of Public Health RE: Classification of Notification Medical Device (Class B and Class C) No. 3 B.E. 2565 2022

The Medical Device Control Division, Thai FDA of the Ministry of Public Health has issued Classification of Notification Medical Device (Class B and Class C) No. 3 B.E. 2565, effective 03 December 2022, repealing The Notification of the Ministry of Public Health RE: Classification of Notification Medical Device (Class B and Class C) B.E. 2563

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Updates

Singapore: Minor Update on GN-06: Guidance on Distribution Records

In line with GDPMDS, HSA Singapore also published minor updates of guidance document entitled GN-06 R3 Guidance on Distribution Records on 01 Nov 2022 which assist product owners on the determination of projected useful life of the medical device. Projected useful life of a medical device is dependent on various factors such as technical, legal,

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New certification

Singapore: GN-33: Guidance on the Application of Singapore Standard Good Distribution Practice for Medical Devices

Health Sciences Authority (HSA) Singapore has reviewed and validated the medical device guidance document entitled GN-33 R1.2 Guidance on the Application of Singapore Standard Good Distribution Practice for Medical Devices Revision 1.2 on 01 Nov 2022 to ensure its accuracy. This guidance document serves to provide advice for application of SS 620: 2016 Singapore Standard

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