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IVDR European Roadshow 2025 – Unveiling the Future of In Vitro Diagnostics.

Next stop: Courbevoie I France  -  September 24th 2025

Join TÜV Rheinland’s in-person, one-day seminar designed exclusively for IVD manufacturers. This event delivers essential knowledge, practical tools, and the latest regulatory insights to help you navigate IVDR compliance with confidence.

Learn directly from TÜV Rheinland experts on certification strategies, technical documentation, performance evaluations, and transitional timelines. Connect with peers, exchange experiences, and get answers to your most pressing compliance questions.

This event is tailored for IVD manufacturers aiming to deepen their understanding of IVDR requirements, certification strategies, and current developments in both the EU and French regulatory landscapes.

Key topics to be covered include:

  • Effective certification strategies under IVDR
  • Preparing technical documentation that passes review
  • Conducting performance evaluations & PMPF
  • Navigating transitional timelines & international approvals

Event Location:
Courbevoie, France | TUV Rheinland France SAS. 20 ter rue de Bezons CS 60030. 92415 Courbevoie cedex

Date: September 24th 2025

Language: English

Meet our Experts

Daniel Świątko
Daniel Świątko
Regional Business Field Manager Medical
Responsible for the development of the medical certification and testing business in Europe. An experienced auditor and certification expert in both active and non-active medical devices.
Agnieszka Topolska-Woś
 Agnieszka Topolska-Woś
IVD Medical Devices Specialist, Lead Auditor
Auditor and expert in in vitro medical diagnostics devices. Many years of experience in the medical devices industry.

Agenda

Morning

09:00 - 09:20
Welcome by TÜV


09:20 - 10:30
Certification strategy IVDR


10:30 - 10:45
Coffee Break


10:45 - 11:30
Guidance for IVDR Technical Documentation


11:30 - 12:15
Performance evaluation and PMPF


12:15 - 13:00
Lunch Break


Afternoon

13:00 - 14:00
International Approvals and IVDR Article 16.
A practical alternative for distributors, manufacturers and importers using the OEM–PLM procedure.


14:00 - 14:30
Q&A session


14:30 - 15:00
Coffee Break


15:00 - 15:30
IVD device testing


15:30 - 16:00
Transitional timelines according to 2024/1860


16:00 - 16:15
Q&A session


16:15 - 16:30
Closing and thanking the participants


We invite you to register here for this unique seminar
Participation Fee: 49 €
Given the limited room capacity - we will limit to maximum 2 participants per company.
You will receive confirmation of your participation within a few days after submitting the form.
By registering for our  seminar, you agree to receive confirmations, reminders and emails regarding it, including documents, videos and presentations, as well as to be contacted by sales representatives on related topics.

Choose Your City to Experience an Engaging Day of Insights and Networking!

Our roadshow is making its way to two additional international locations—be one of the first to register !

Seats are limited — secure your spot early!

Pricing and seats:
Participation fee: 49 €


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Language: English
Register for Leiden

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