Please make sure to enhance your regulatory knowledge and strengthen your understanding of medical devices and in vitro diagnostic medical devices (IVDs) under the Malaysian Medical Device Act 2012 (Act 737).

This one-day training provides comprehensive exposure to risk-based classification principles, determination of intended purpose, differentiation between medical, non-medical, and combination products, as well as the practical classification of rehabilitation, physiotherapy, and speech therapy devices in accordance with Malaysian and ASEAN regulatory requirements.

Participants will gain hands-on experience through case studies and scenario-based exercises, enabling accurate classification and avoidance of common misclassification pitfalls faced by the industry.

Date: 28 January 2025 (Wednesday)
Time: 8:45 a.m. – 5:00 p.m.
Venue: Seminar Room, Level G, Medical Device Authority (MDA), Cyberjaya
Fee: RM1,000 per participant
Target Audience: Industry Regulatory & Technical Personnel
Registration Deadline: Before 20 January 2026

This program is HRD Corp claimable under the SBL Scheme.

👉For more information, please click the link as follows:   The Training of Fundamental Understanding of Medical Devices & IVDs

👉 Register now to secure your place.

Prepared by: MDA CORE (Administrative Division)

Uploaded by: Corporate Communication Division

Date of upload: 15 January 2026