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49 pages. Presented by Ms. Salbiah Yaakop. 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 presentation outlined the WHO Regulatory Model (pre-market, placing on-market and post-market surveillance), the regulatory activities involved in Act 737 and medical device registration.
Ms. Salbiah Yaakop (Medical Device Authority, Malaysia)
Publication Date:9 February 2018
Category/Type: Seminar Papers/PDF
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