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15 pages. Presented by Ir. Sasikala Devi. Briefing on OEM Licensing and Product Registration Requirements for Certificate of Free Sales (CFS) Issuance was held on 9th February 2018 at MREPC Seminar Hall, Kuala Lumpur. The briefing provided an overview of Medical Device Authority and its function, the flow of institutional structure in Medical Device Act 2012 and regulatory updates of Act 737. Prohibition Order and Medical Device Act 2012 transitional period was also discussed.
Ir. Sasikala Devi (Medical Device Authority, Malaysia)
Publication Date:9 February 2018
Category/Type: Seminar Papers/PDF
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