Quality management system according to EN ISO 13485. 09397 -
Seminar / Kurs
von TÜV Rheinland Akademie GmbH
Understand, interpret and implement requirements of EN ISO 13485:2016 for the medical device industry.
The EN ISO 13485 is the basis for QM systems in the medical device industry. EN ISO 13485:2016 defines new requirements for medical device manufacturers and specifies the requirements of the predecessor standard. Get to know the structure and contents of EN ISO 13485:2016 and learn how to set up or adapt your QM system accordingly.
Structure, (new) requirements of EN ISO 13485:2016/AC:2016EN ISO 13485:2016/AC:2016 and the specific national, regional or international regulatory requirements for medical device manufacturersIntegration of risk management in the QM system or in the company processes including outsourced processes and the entire product life cycleSelection and ongoing evaluation of suppliersDocumentation structure and evidence documentsValidation, verification, design transferdealing with complaintsFeedback and reportingMajor differences to EN ISO 13485:2012+AC:2012Audits and inspections according to EN ISO 13485:2016/AC:2016 by the notified body or competent authorities - EN ISO 13485:2016/AC:2016 versusMDR (Medical Device Regulation)ISO 13485 as the basis for the global Medical Device Single Audit Program (MDSAP)Tipps for implementing EN ISO 13485:2016/AC:2016 in your company
You will learn about the structure, contents and requirements of EN ISO 13485:2016/AC:2016 as well as the main differences to the previous version EN ISO 13485:2012+AC:2012.You know how to introduce a QM system based on EN ISO 13485: 2016/AC:2016 or how to adapt your own quality management system to the new requirements.You benefit from concrete practical examples that make it easier for you to implement or adapt your system.
The seminar is suitable for employees who are or will be responsible for the implementation of EN ISO 13485 in medical device companies.
Termine und Orte