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Tajuk	Dikunjungi
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 2 YEAR 2018 (REVISION 2) : CONTROL OF ORPHANED, OBSOLETE AND DISCONTINUED MEDICAL DEVICE IN HOSPITAL, HEALTHCARE FACILITIES INSTITUTION OR ANY RELATED FACILITIES	Dikunjungi: 11213
GUIDANCE DOCUMENT : MDA/GD/0018: IMPORT AND/OR SUPPLY OF UNREGISTERED MEDICAL DEVICES FOR THE PURPOSE OF DEMONSTRATION FOR MARKETING OR EDUCATION	Dikunjungi: 14208
MEDICAL DEVICE (ADVERTISING) REGULATIONS 2019 AND MEDICAL DEVICE (DUTIES AND OBLIGATIONS OF ESTABLISHMENTS) REGULATIONS 2019	Dikunjungi: 21133
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 1 YEAR 2019 (REVISION 1) POST-MARKET RESPONSIBILITIES FOR MANUFACTURER AND AUTHORIZED REPRESENTATIVE (AR)	Dikunjungi: 13392
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	Dikunjungi: 11711
AWARENESS PROGRAM FOR NON-CORRECTIVE CONTACT LENS	Dikunjungi: 19735
MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION	Dikunjungi: 46696
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	Dikunjungi: 13922
Medical Device Authority announces the rebranding of Industrial Support Unit as MDA-CoRE	Dikunjungi: 14078
PENAMATAN BADAN PENILAIAN PEMATUHAN (CAB)	Dikunjungi: 9661