• Home
  • Announcement
  • TRAINING BY THE AUTHORITY: - COMPULSORY COMPETENCY MODULE (REGULATORY REQUIREMENTS) FOR BIOMEDICAL TECHNICAL PERSONNEL

TRAINING BY THE AUTHORITY: - COMPULSORY COMPETENCY MODULE (REGULATORY REQUIREMENTS) FOR BIOMEDICAL TECHNICAL PERSONNEL

Just Released
This is to announce that the training for competency module (regulatory requirements) for biomedical technical personnel is now open for registration.

New course for BTP

INTRODUCTION
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.

OBJECTIVES
• 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

TARGET AUDIENCE
• Biomedical Technical Personnel
• Biomedical Service Provider
• Biomedical Engineering Trainers
• Students and fresh Biomedical, Mechanical, Mechatronics, Electrical, Electronics Engineering graduates
• Technical and Vocational Education and Training (TVET)
• BEM and FEM Managers
• Lecturers

TENTATIVE

TRAINING BY THE AUTHORITY: - COMPULSORY COMPETENCY MODULE (REGULATORY REQUIREMENTS) FOR BIOMEDICAL TECHNICAL PERSONNEL

Date (Day)

:

13 NOVEMBER 2019 (Wednesday)

Time

:

8.00 AM – 5.30 PM

Venue

:

MEDICAL DEVICE AUTHORITY, BILIK SEMINAR 1 & 2, LEVEL G, PRIMA 9, PRIMA AVENUE II, BLOCK 3547, PERSIARAN APEC, 63000 CYBERJAYA 63000 CYBERJAYA

TENTATIVE

8.00am - 8.55am

 

Registration & Breakfast

9.00am - 10.30am

 

Medical Device Act 2012, Act 737

10.30am - 10.45am

 

Refreshment

10.45am - 11.45am

 

Medical Device Regulatory Requirement in Healthcare Institution and Private Healthcare Act, Act 586

11.45am – 12.45am

 

Atomic Energy Licensing Act, Act 304

12.45pm – 2.00pm

 

Lunch

2.00pm-3.00pm

 

Occupational, Safety and Health Act, Act 514

3.00 pm – 4.00pm

 

Disposal of Medical Device Requirements

4.00 pm - 5.00pm

 

Examination

5.00pm – 5.30pm

 

Afternoon Tea, End

To register, please click HERE

Kindly  complete the provided Registration Form and submit to trainingpackage@mda.gov.my. An invoice (for payment purpose) will be issued accordingly, upon the acceptance of the Registration Form. The closing date for registration is on 1st November 2019.

Should you have any enquiries, please do not hesitate to email us at trainingpackage@mda.gov.my

Print

  Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

  +603 - 8230 0300
  +603 - 8230 0200 
  mdb@mda.gov.my