The Malaysian Medical Devices Authority (MDA) has announced that all COVID-19 test kits whether for professional use or for personal use must be registered under Section 5 of the Medical Devices Act 2012 (Act 737) before being placed on the market. This is effective as of 1 February 2022. New guidelines on registering Covid-19 test kits can be found on the MDA website.
Victoria Caldy
Andaman Medical
victoria@andamanmed.com
andamanmed.com
Regulatory Affairs & Market Access for Southeast Asia------------------------------
Victoria Caldy
Marketing & Business Development Director
Singapore
Singapore
------------------------------