This course is designed to provide participants with the practical knowledge to comply with the ISO 13485:2016 medical devices quality management system requirements.
By the end of this course, participants will be able to:
Understand the key changes in the regulatory requirements of ISO 13485:2016.
Interpret and apply the revised requirements of ISO 13485:2016, clause by clause, in a practical manner.
Comply with the ISO 13485:2016.
Date: 10th July 2017
Venue: SMT Technologies Sdn. Bhd., Sungai Petani, Malaysia
Who Must Attend:
Individuals with ISO 13485 responsibility, in particular Managers, Engineers, Exempt-staffs, and Internal Auditors.
Feel free to contact TSY Consultancy by Call / WhatsApp to +6017-4036965 or email to email@example.com