Online workshop: Requirements of Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices
14. 03. 2024
What are in vitro diagnostic (IVD) medical devices?
VD medical devices are tests used on biological samples (such as tissue, blood, or urine) to determine a person's health. There is a very wide range of IVD medical devices, from pregnancy self-testing aids, blood glucose meters to HIV tests, blood group tests and various types of cancer tests. Unlike medical devices or IVD pharmaceuticals, medical devices never come into contact with a person and do not treat patients but provide information about the functioning of the body. IVD medical devices do not cause direct harm, but they pose a very high risk if their use leads to misdiagnosis. A detailed definition of IVD medical devices is given in Regulation (EU) 2017/746, Article 2.
The IVDR replaced the IVDD (In Vitro Diagnostic Medical Devices Directive 98/79/EC) on 26 May 2022 and applies in all EU Member States and EFTA countries. This means that economic operators wishing to obtain the CE marking for their products or to market their products in Europehave to comply with a new set of stricter, more demanding and more complex requirements with which their products must comply. With the IVDR, the European Commission aims in particular to create a robust, transparent, sustainable and internationally recognised regulatory framework that will improve the clinical safety, quality and reliability of IVD medical devices and ensure fair market access for manufacturers, healthcare professionals and end-users.
This means that economic operators wishing to receive the CE mark for their products or to market their products in Europe will encounter a new set of requirements that are generally stricter, more demanding, more complex, and time-consuming than those currently required to comply with. With the IVDR, the European Commission wants to create a solid, transparent, sustainable, and internationally recognized regulatory framework that will improve the clinical safety, quality and reliability of IVD medical devices and ensure fair market access for manufacturers, healthcare professionals and end-users.
At the seminar, we will present the new requirements of Regulation (EU) 2017/746 which are important for manufacturers, authorized representatives, importers and distributors of in vitro diagnostic medical devices in the European Union, and for professionals involved in quality management systems, including IVD medical devices.
Overview of Regulation (EU) 2017/746 and definitions
Obligations of economic operators
Classification and conformity assessment
Safety and efficacy requirements (Annex I – GSPR)
Requirements for technical documentation
Unique Identification System (UDI) and EUDAMED
Post-market surveillance and vigilance
Course and materials will be in English language.
Marjeta Tušek Jelenc is a university graduate in physics. She began her professional career as a researcher at the Medical University of Vienna, where she was involved in the development of a new magnetic resonance method. In 2017, she joined SIQ Ljubljana as a professional associate in the field of medical device certification. Since April 2021, he has been employed by the Swiss company Smart Blood Analytics Swiss SA, where they develop software for in vitro diagnostic medical devices and is responsible for their compliance with relevant legislation. She is a SIQ auditor for ISO 9001, ISO 13485 and MDR.
The online workshop will take place in a live online e-classroom and will be divided into three parts with breaks in between. 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.