- Introducing Medical Device & ISO 13485 :2016
- Interpretation on the requirements and implementation of ISO 13485:2016
- Interpretation of key ISO 13485:2016 clauses
- To understand the concept behind and application of the standards
- To introduce ISO 13485 :2016 requirements
WHO SHOULD ATTEND?
- Person in charge of establishing and Implementing ISO 13485
- Management Representatives
- Person is seeking for learning essential knowledge in quality management control in medical device industry
- Medical Device professionals interested in conducting first party, second party, and/or third party audits
CERTIFCATE AND CPD:
Certificate of successful Completion will be awarded delegates who have attended full course. An e-Certificate will only be granted. You may be able to claim CPD hours for your membership at professional bodies.
** RTTP (Reindustrialisation and Technology Training Progamme) Recognized Training Course **
RTTP Pre-approval training courses, eligible company could apply for RTTP funding in order to receive up to 2/3 course fee reimbursement for each employee.