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NEW RELEASE GUIDELINE DOCUMENT MDA/GL/10: GUIDELINE DOCUMENT ON HOW TO SUBMIT AN APPLICATION FOR REGISTRATION OF A REFURBISHED MEDICAL DEVICE	Hits: 7525
Fifth Edition Guideline for Medical Device-Drug and Drug-Medical Device Combination Product	Hits: 7503
PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO)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	Hits: 7352
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS	Hits: 6806
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information	Hits: 10922
PINDAAN TERKINI SYARAT-SYARAT LESEN	Hits: 9382
FOURTH EDITION GUIDANCE DOCUMENT MDA/GD/0020: CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE	Hits: 10843
SIXTH EDITION GUIDANCE DOCUMENT MDA/GD/0026: REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES	Hits: 10335
TRAINING FOR RE-REGISTRATION FOR CAB AUDITORS AND TECHNICAL PERSONNEL UNDER ACT 737 (COMPLIANCE TO THE CONFORMITY ASSESSMENT BODY REGISTRATION REQUIREMENTS)	Hits: 12465
TRAINING BY THE MEDICAL DEVICE AUTHORITY ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICE (GDPMD) FOR LEAD AUDITOR	Hits: 15524