Malaysia MDA: Training by the Authority – Compulsory Competency Module (Regulatory Requirements) For Biomedical Technical Personnel

November 1, 2019

MDA announced the training for competency module (regulatory requirements) for biomedical technical personnel.

 

The 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.

 

Malaysia aims to: 

• 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

 

Reference: Malaysia MDA

 

Contact us at info@arqon.com.

 

 

 

 

 

 

 

 

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