EU Medical Device Regulation (MDR) 2017/745 – QMS Auditor - International

Niveau Spécialiste Durée 3 journées de formation

Disponible pour réserver: Salle de classe virtuelle 2560€ + TVA Book your place

The Medical Device Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

As more and more manufacturers now have their MDR Quality Management System (QMS) certificates, it’s imperative for continued compliance that they are able to perform audits against the requirements of the QMS MDR.

This course is designed to give you insights into how Notified Bodies may perform an MDR QMS compliance audit, using the topics of a typical MDR audit agenda as the basis. This will enable you to optimize your auditing skills and knowledge to boost your audit capabilities, gain confidence in planning and performing an effective EU MDR QMS audit, as well as ensuring continued compliance to the EU MDR (2017/245).

Please note that this training will be held in English!

Prerequisites

Already a competent auditor in the medical device industry and especially familiar with the auditing requirements of ISO 13485:2016.

You must have a good understanding of the requirements of the MDR. You should also have experience with quality management systems for the medical device industry. Recommended to have either attended the ISO 13485 Lead auditor or ISO 13485 internal auditor course.

Pedagogical objectives

Perform audits against the EU MDR (2017/245) Quality Management System requirements
Ensure continued compliance against the EU MDR (2017/245) QMS requirements
Be confident that your organization can rely on competent EU MDR (2017/245) auditors

- RA, QM, and QA professionals who already perform audits
- Anyone concerned with certification or active in projects for CE-marking, especially involved in the QMS implementation side
- Staff involved in audits and working for organizations that partner with Medical Device manufacturers e.g. as subcontractor, crucial supplier, OEM, Authorized representative, importer, distributor, auditee
By the end of the course you’ll be able to:
- Establish the relationship between the ISO 13485:2016 and the EU MDR (2017/745)
- Recognize and interpret the key QMS requirements of the EU MDR (2017/745)
- Appreciate that the range of medical device classifications mean differing requirements in the context of auditing
- Plan for and conduct EU MDR (2017/745) QMS audits to establish and maintain compliance against these requirements
- Report on any identified nonconformities
- Questionnaire to assess the knowledge at the end of the training
- Customer survey
- Course materials, provided electronically
- Letter of attestation
- Official certificate
Course materials including :
- Introduction to the training, detailed programme and security assignments
- Course presentation, theory and activities/ role plays
- Answers to the activities
- Videos
- Additional documents, distributed during the sessions, to use for the activities
- Attendance sheet to be signed
This guide will give you all the necessary information.
Download our training guide: EU Medical Device Regulation (MDR) 2017/745 – QMS Auditor (International)
* These training modules are eligible to the subsidizing by the public institutions in France (OPCO).

**Each delegate receives a training convention after enrollment.

***Please note that for the public sessions, you have until 48h before the start of the course to confirm your enrollment. For the in-house sessions, the deadline would be of two weeks prior to the start of the course.

****Should you be in a disabled situation, please contact us and indicate what details should be taken into account.

You can contact us on training.france@bsigroup.com or 01 89 79 00 40.

Nous contacter

Travaillons ensemble pour bâtir l'avenir de votre organisation

Contactez-nous pour découvrir comment nous pouvons vous aider à réussir

Nous contacter