MDA's e-Training: All courses

Course categories:

16 JULY 2024 - REGULATORY TRAINING : POST-MARKET REQUIREMENTS

19 th October 2023 – Medical Device Seminar by The Medical Device Authority

12 Oktober 2022 - Seminar By The Medical Device Authority on Regulatory Updates in Putrajaya

5 Julai 2022 - Seminar by The Medical Device Authority on Regulatory Updates (Penang)

LATIHAN RE-REGISTRATION EVALUATION PROCEDURE AND REQUIREMENT FOR CAB

31 Mac 2022 - Seminar by The Authority: Regulatory Updates And Facilitation Towards Addressing The Challenges Of Covid-19 Pandemic

Medical Device Webinar 2020: New Medical Device Regulations Under Act 737: Advertisement And Post Market Requirements - August 17, 2020

MEDICAL DEVICE WEBINAR 2021 POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737: ADVERTISEMENT, POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE-REGISTRATION - 03 MARCH, 2021

MEDICAL DEVICE WEBINAR 2021 POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737: ADVERTISEMENT, POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE-REGISTRATION - 10 JUNE, 2021

MEDICAL DEVICE WEBINAR 2021: POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737: ADVERTISEMENT, POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE-REGISTRATION - 6 OCTOBER, 2021

Program Kesedaran Pengguna Akta Peranti Perubatan 737 (PBPP) 2021

Program MEDICAL DEVICE WEBINAR 2021: POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737: ADVERTISEMENT, POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE-REGISTRATION -11 AUGUST, 2021