If you change your Authorised Representative in Malaysia, your device registration does not automatically follow. This guide explains what the outgoing AR controls, what happens if they will not cooperate, and the contractual protections foreign manufacturers should put in place before appointing.
How NPRA decides whether a product is a cosmetic in Malaysia, using the five-step decision process in the Guideline for Cosmetic Claims. Covers permitted secondary functions, acceptable and unacceptable claims by product type, and the wording that most often pushes an imported product out of the cosmetic category.
A guide to Malaysia's cosmetic ingredient annexes under NPRA and the ASEAN Cosmetic Directive, covering which annexes apply, how they are updated, transition periods for notified products, and how to screen a formula before manufacturing.
A practical guide to NPRA cosmetic labelling requirements in Malaysia for imported products, covering the nine mandatory particulars, ingredient listing rules, animal origin declaration, expiry dating, small packaging exemptions, and a pre-print checklist.
Learn how cosmetic notification works in Malaysia under NPRA and the ASEAN Cosmetic Directive. Understand who can be a Cosmetic Notification Holder, what the Quest 3+ process involves, labelling and PIF requirements, and why brand owners should think carefully about who holds the notification.
Learn how foreign medical device manufacturers can appoint a Malaysia medical device license holder or authorized representative to support MDA registration, distributor appointment, market entry, and post-market compliance.
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