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PERLUASAN PENJUALAN KIT UJIAN KENDIRI COVID-19 DI PREMIS-PREMIS YANG MEMENUHI SYARAT-SYARAT DAN KEPERLUAN YANG DITETAPKAN 02 November 2021 9080
CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY 2 YEAR 2014 (APPENDIX 1-REVISION 4) 25 October 2021 15001
UPDATES ON GUIDELINE FOR REGISTRATION OF DRUG-MEDICAL DEVICE AND MEDICAL DEVICE-DRUG COMBINATION PRODUCTS 4TH EDITION 25 October 2021 9108
KENYATAAN MEDIA PERLUASAN PENJUALAN KIT UJIAN KENDIRI COVID-19 15 October 2021 11029
TRAININGS ON ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES - 10 & 11 NOVEMBER 2021 12 October 2021 13781
COMPULSORY COMPETENCY MODULE: INTRODUCTION TO REGULATORY REQUIREMENTS FOR BIOMEDICAL TECHNICAL PERSONNEL (BTP) 11 October 2021 13488
TRAININGS FOR CONFORMITY ASSESSMENT BODY (TRAININGS SANCTIONED BY THE MEDICAL DEVICE AUTHORITY) 21 September 2021 15948
PEMBATALAN SURAT PEKELILING PIHAK BERKUASA PERANTI PERUBATAN (PBPP) BIL 1/2014 14 September 2021 17442
MEDICAL DEVICE WEBINAR 2021 - POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737 : ADVERTISEMENT , POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE- REGISTRATION 07 September 2021 11494
REQUIREMENTS FOR REGISTRATION MEDICAL GAS SYSTEM - AWARENESS PROGRAM 20 August 2021 8421

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Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
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