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Tajuk	Tarikh diterbitkan	Dikunjungi
NEW RELEASE GUIDELINE DOCUMENT MDA/GL/10: GUIDELINE DOCUMENT ON HOW TO SUBMIT AN APPLICATION FOR REGISTRATION OF A REFURBISHED MEDICAL DEVICE	11 Januari 2023	Dikunjungi: 7848
Fifth Edition Guideline for Medical Device-Drug and Drug-Medical Device Combination Product	11 Januari 2023	Dikunjungi: 7806
PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO)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: 7681
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS	16 Disember 2022	Dikunjungi: 7109
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information	14 Disember 2022	Dikunjungi: 11227
PINDAAN TERKINI SYARAT-SYARAT LESEN	13 Disember 2022	Dikunjungi: 9791
FOURTH EDITION GUIDANCE DOCUMENT MDA/GD/0020: CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE	21 November 2022	Dikunjungi: 11355
SIXTH EDITION GUIDANCE DOCUMENT MDA/GD/0026: REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES	21 November 2022	Dikunjungi: 10907
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: 12793
TRAINING BY THE MEDICAL DEVICE AUTHORITY ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICE (GDPMD) FOR LEAD AUDITOR	31 Oktober 2022	Dikunjungi: 15780