SIQ: Online training course: Traceability of medical devices and manufacturers‘ obligations in relation to post-market activities (Regulation (EU) 2017/745)

This workshop will be in English and is part of our new academy cooperation with the Slowenian notified body SIQ!

About the training

This training course will present the requirements of the new Regulation (EU) 2017/745 on Medical Devices, focusing on the regulatory requirements for manufacturers and other business entities after placing medical devices on the market. We will discuss all post-market monitoring activities and learn about the requirements for ensuring the traceability of medical devices. The main purpose of the new requirements of the Regulation is to ensure that only safe and effective medical devices are used in the Common European Market and beyond.

Participants will learn about the most important changes to requirements for traceability and post-market monitoring of medical devices brought by Regulation (EU) 2017/745.


  • Overview of the basic differences between the MDD and the MDR in the area of traceability
  • New requirements for medical device manufacturers
  • New developments in the area of requirements for medical devices
  • Explanation of the regulatory requirements for participating legal entities
  • Ensuring the traceability of medical devices and their labelling
  • Post-market monitoring and reporting obligations


  • Standard: 475,00 EUR (excl. VAT)
  • Get your special 10 % with this code: encosiq10
  • incl. seminar documents as PDF and a certificate of participation.

Your Trainer

Marjetka Kralj Kunčič PhD is a Doctor of Science in microbiology with more than 17 years of experience in quality management systems. Her previous work with a medical device manufacturer included not only laboratory management and quality control, but also active involvement in the development, production and regulatory compliance of medical devices, as well as quality management system compliance. Currently, she works as an SIQ auditor and a consultant in the field of medical devices and a member of the technical group for the preparation of health protection standards.

Location: ONLINE

The online workshop will take place in a live online e-classroom. Up to two days before the implementation, registered participants will receive a link to the online training. Participants need a computer with a microphone and a camera, as well as access to a reliably functioning internet connection to participate in online training without interruption.

Click here to book now!

Don’t forget to use this code for a special 10 % encosiq10

For questions please text: or call +43 1 8863491

This workshop will be in English and is part of our new academy cooperation with the Slowenian notified body SIQ!