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Tajuk	Tarikh diterbitkan	Dikunjungi
Fifth Edition Guideline for Medical Device-Drug and Drug-Medical Device Combination Product	11 Januari 2023	Dikunjungi: 7753
PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO) MEDICAL DEVICES	23 Disember 2022	Dikunjungi: 7640
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS	16 Disember 2022	Dikunjungi: 7064
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information	14 Disember 2022	Dikunjungi: 11172
PINDAAN TERKINI SYARAT-SYARAT LESEN	13 Disember 2022	Dikunjungi: 9726
FOURTH EDITION GUIDANCE DOCUMENT MDA/GD/0020: CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE	21 November 2022	Dikunjungi: 11258
SIXTH EDITION GUIDANCE DOCUMENT MDA/GD/0026: REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES	21 November 2022	Dikunjungi: 10799
TRAINING FOR RE-REGISTRATION FOR CAB AUDITORS AND TECHNICAL PERSONNEL UNDER ACT 737 (COMPLIANCE TO THE CONFORMITY ASSESSMENT BODY REGISTRATION REQUIREMENTS)	01 November 2022	Dikunjungi: 12739
TRAINING BY THE MEDICAL DEVICE AUTHORITY ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICE (GDPMD) FOR LEAD AUDITOR	31 Oktober 2022	Dikunjungi: 15746
PUBLIC COMMENT DRAFT MEDICAL DEVICE GUIDANCE DOCUMENT NOTIFICATION FOR CUSTOM-MADE MEDICAL DEVICE	31 Oktober 2022	Dikunjungi: 7660