Seminar

New IVDR regulation explained for developers of in-vitro diagnostic medical devices

26 May 2022 is the official date of application for the Regulation 2017/746 on in vitro diagnostic medical devices (IVDR), thereby repealing the old IVD directive 98/79/EC. There are still many obstacles to overcome and unclarities to address for IVD manufacturers and suppliers to the IVD industry. During this session, an expert in the IVD field from Qarad will provide insights into these regulations and you will have the opportunity to ask questions related to your specific project or situation.

Within the context of the next supervisory group meeting of the COOCK project 'Medical diagnostics goes micro and smart' a seminar will be organised by one of the member companies. This part of the meeting will therefore be open to third parties and companies not involved in the project.

During this seminar we will focus on the application of the Regulation on microfluidic chips and on their conditioning and read-out devices meant for diagnostic testing.

Further information on the speaker (Qarad) and the IVDR regulation can be found on our blog

For whom?

The seminar is aimed at companies manufacturing the systems and accessories for such in-vitro diagnostic medical devices, including their suppliers and service providers.

Participants fee

The seminar is free for members of the supervisory group of the COOCK project 'Medical diagnostics goes micro and smart'. Other participants pay 200 euro (excl. VAT).