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CAB PROFICIENCY TRAININGS FOR NEW / FRESH PERSONNEL SANCTIONED BY THE MEDICAL DEVICE AUTHORITY ORGANIZED FROM MARCH 13, 2023 TO MARCH 16, 2023 21 Februari 2023 10824
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 8407
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PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO)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 8397
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS 16 Disember 2022 7698
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information 14 Disember 2022 11839
PINDAAN TERKINI SYARAT-SYARAT LESEN 13 Disember 2022 10925
FOURTH EDITION GUIDANCE DOCUMENT MDA/GD/0020: CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE 21 November 2022 12202
SIXTH EDITION GUIDANCE DOCUMENT MDA/GD/0026: REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES 21 November 2022 12011
TRAINING FOR RE-REGISTRATION FOR CAB AUDITORS AND TECHNICAL PERSONNEL UNDER ACT 737 (COMPLIANCE TO THE CONFORMITY ASSESSMENT BODY REGISTRATION REQUIREMENTS) 01 November 2022 13349

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