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MDA-CORE 2025
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MDA-CORE 2025
Course categories:
CAB
CAB / CAB_2024
GDPMD
Hands On Workshop
MED
Seminar
Set Soalan Temuduga
Set Soalan Temuduga / Set Soalan Temuduga F41
Set Soalan Temuduga / Set Soalan Temuduga FA29
Software
UKK
UKP
ISO
CLINICAL
CAB2023
MDA CORE 2023
TOT
MDA CORE 2024
SEMINAR 2024
BKPP
INTERVIEW
INTERVIEW / FA05_202501
CAB_2025
MDA-CORE 2025
GDPMD 2025
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25 NOVEMBER 2025 - TRAINING ON INTRODUCTION OF MEDICAL DEVICE REGULATORY FRAMEWORK IN MALAYSIA
11 NOVEMBER 2025 - TRAINING ON FUNDAMENTAL OF SOFTWARE AS MEDICAL DEVICE (SAMD)
4 NOVEMBER 2025 - TRAINING ON ISO 14971 : RISK MANAGEMENT SYSTEM FOR MEDICAL DEVICES
29 OCTOBER 2025 - SESSION 2 REGULATORY TRAINING: POST MARKET REQUIREMENTS
8 & 9 OCTOBER 2025 - TRAINING ON ISO 13485:2016 QUALITY MANAGEMENT SYSTEM MEDICAL DEVICE REQUIREMENTS
17 SEPTEMBER 2025 - TRAINING ON IMPORT & EXPORT MEDICAL DEVICE REQUIREMENTS
21 & 22 AUGUST 2025 - TRAINING ON COMPLIANCE ON GDPMD
20 AUGUST 2025 - REGULATORY TRAINING POST MARKET REQUIREMENTS
13 AUGUST 2025 - TRAINING ON CLINICAL EVIDENCE OF MEDICAL DEVICE
23 JULY 2025 - THE TRAINING OF MEDICAL DEVICE LABELLING AND ADVERTISMENT REQUIREMENTS
18 JUNE 2025 - IN DEPTH TRAINING ON IN-VITRO DIAGNOSTIC MEDICAL DEVICE REQUIREMENT
BENGKEL PEROLEHAN PERANTI PERUBATAN : MEMENUHI KEPERLUAN REGULATORI BERDASARKAN AKTA 737
21 MAY 2025 - TRAINING ON IMPORT AND EXPORT OF MEDICAL DEVICE REQUIREMENTS
14 MAY 2025 - IN DEPTH TRAINING ON GENERAL MEDICAL DEVICE
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