TSY In House Training #12: Transition to ISO 13485:2016 Medical Device Quality Management System

Updated: Jul 12, 2018


TSY In House Training #12: Transition to ISO 13485:2016 Medical Device Quality Management System
Trainer explaining the differences between the new and previous ISO 13485.

This course is designed to provide participants with the practical knowledge to comply with the ISO 13485:2016 medical devices quality management system requirements.


Course Objectives:

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 marketing@tsy.my


Cheers.


#TSYConsultancy #ISO13485ver2016 #AwarenessOnISOChanges #InHouseTraining #HRDFClaimable #SungaiPetani

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