12 February 2020 (Wednesday) | 8.00 AM – 5.30 PM (TRAINING) 13 February 2020 (Thursday) | 8.00 AM – 10.30 AM (EXAMINATION)
Medical Device Authority, Bilik Meranti, Level 6, Prima 9, Prima Avenue II, Block 3547, Persiaran Apec, 63000 Cyberjaya
This regulatory module is designed to provide participants with the knowledge on medical device regulatory requirements in Malaysia. Biomedical technical personnel, supervisors and managers responsible for maintenance, testing & commissioning and disposal of medical device in Healthcare Institution and related facilities will benefit from this course. Participants will gain an overview of the requirements of the Medical Device Regulation, Medical Device in Healthcare Institution, Act 586, Act 304, OSHA, and Disposal.
· Obtain an overview of the Medical Devices Act, Act 586, Act 304, OSHA and Disposal
· Understand the medical device regulatory requirements in healthcare and related facilities
· Biomedical Service Provider · Biomedical Technical Personnel · Biomedical Engineering Trainers · Biomedical, Mechanical, Mechatronics, Electrical, Electronics Engineering graduates · Technical and Vocational Education and Training (TVET) · BEM and FEM Managers · Lecturers
REGISTRATION AND TRAINING FEE
Training fee for per participant: RM 750
· Inclusive of refreshments, lunch (12 February 2020), training materials, examination & certificate · No meal will be provided on the examination day (13 February 2020) · Training fee does not include accommodation & travelling costs
Kindly complete the provided Registration Form and submit to email@example.com. An invoice (for payment purpose) will be issued accordingly, upon the acceptance of the Registration Form. The closing date for registration is on 1st February 2020.
To register, please download Attachment 1.
Source: MDA Malaysia
Contact ARQon at firstname.lastname@example.org