The Medical Device Centralized Reporting System is a simple online application that can be used by the establishment to inform the Authority about their post marketing activities, namely a Mandatory Problem Reporting, a Field Corrective Action activity and also a Recall action.
Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA
+603 - 8230 0300
+603 - 8230 0200
mdb@mda.gov.my
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