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Guideline, Guidance and Circular letter PDF Print E-mail

Guidance Documents are prepared to assist in the  governing statutes and  regulations under the Medical Device Act 2012  (Act 737) interpretation of policies.

Guidelines are prepared to assist industries and healthcare faciities during implementation of medical device regulatory system.

We are pleased to inform that MDA has decided on new policies to facilitate the stakeholder and industry in the implementation of Medical Device Act (Act 737). 



Last Updated ( Tuesday, 23 February 2016 )
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