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CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 1 YEAR 2019 (REVISION 1) POST-MARKET RESPONSIBILITIES FOR MANUFACTURER AND AUTHORIZED REPRESENTATIVE (AR)	Hits: 12520
Unrecognise Training Provided By Other Parties Other Than Medical Device Authority In Relation To The Medical Device Act 2012 (Act 737) And Medical Device Regulatory Requirements	Hits: 10768
AWARENESS PROGRAM FOR NON-CORRECTIVE CONTACT LENS	Hits: 17122
MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION	Hits: 39800
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 2 YEAR 2018 REVISION 1 : CONTROL OF ORPHANED, OBSOLETE AND DISCONTINUED MEDICAL DEVICE IN HOSPITAL, HEALTHCARE FACILITIES INSTITUTION OR ANY RELATED FACILITIES	Hits: 13048
Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE	Hits: 13155
DISCONTINUATION OF CONFORMITY ASSESSMENT BODY (CAB)	Hits: 8840
APPLICATION FOR NOTIFICATION OF EXPORT ONLY MEDICAL DEVICE	Hits: 10237
NEW RELEASE GUIDANCE DOCUMENT MDA/GD/0051:GUIDANCE DOCUMENT ON NOTIFICATION OF EXPORT ONLY MEDICAL DEVICE	Hits: 7027
PELETAKAN DALAM PASARAN DAN PENGGUNAAN PERANTI YANG TIDAK BERDAFTAR DAN TIDAK MEMPUNYAI BUKTI KLINIKAL	Hits: 7510