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Tajuk	Dikunjungi
Fifth Edition Guideline for Medical Device-Drug and Drug-Medical Device Combination Product	Dikunjungi: 7500
PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO)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	Dikunjungi: 7352
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS	Dikunjungi: 6805
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information	Dikunjungi: 10919
PINDAAN TERKINI SYARAT-SYARAT LESEN	Dikunjungi: 9380
FOURTH EDITION GUIDANCE DOCUMENT MDA/GD/0020: CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE	Dikunjungi: 10843
SIXTH EDITION GUIDANCE DOCUMENT MDA/GD/0026: REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES	Dikunjungi: 10331
TRAINING FOR RE-REGISTRATION FOR CAB AUDITORS AND TECHNICAL PERSONNEL UNDER ACT 737 (COMPLIANCE TO THE CONFORMITY ASSESSMENT BODY REGISTRATION REQUIREMENTS)	Dikunjungi: 12460
TRAINING BY THE MEDICAL DEVICE AUTHORITY ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICE (GDPMD) FOR LEAD AUDITOR	Dikunjungi: 15519
PUBLIC COMMENT DRAFT MEDICAL DEVICE GUIDANCE DOCUMENT NOTIFICATION FOR CUSTOM-MADE MEDICAL DEVICE	Dikunjungi: 7426