Changes and impacts of the new EU IVD regulatory requirements with CDx specifics

Tuesday, June 13th 2017, 17:00 CET | 11:00 EDT
Voisin Consulting Life Science - 64, Avenue Pierre Grenier, 92100 Boulogne

Presenters: Sylvie Le Glédic, Director, Medical Devices & IVD

Date:          June 13, 2017

Duration:    45 Minutes

Time:          17:00 CET / 11:00 EDT / 08:00 PDT

The new EU IVD regulation will introduce major changes that will greatly impact IVD product development and CE marking. These changes will introduce delay to market access and increased cost to CE marking IVD medical devices in Europe. As an example, there will be a premarket review of technical dossiers by a Notified Body for the majority of the devices.

In particular, companion diagnostics (CDx) will be classified as high risk devices which would necessitate the involvement of Notified Bodies prior to CE Marking, unlike the current situation. This regulatory body will assess the CDx documentation and the manufacturers’ quality system before issuing the EC design examination certificate.

However, this premarket review of IVD/CDx documentation and manufacturer’s quality system might provide more recognition of the CE mark outside Europe where CE mark of IVDs is today considered a low value, as CE self-certification applies to the vast majority of IVDs, including CDx.

This presentation describing the new EU regulatory framework for IVDs and companion diagnostic will discuss some essential topics related to CE marking according to the new EU requirements: device classification and conformity assessment, the importance of the demonstration of the clinical evidence to be included in the CE technical documentation, future interactions between the EMA and the Notified Bodies involved in CE marking of CDx.

Key learning objectives:

  • Understanding the future EU IVD regulatory framework

  • Key development activities for CE marking IVDs/CDx

  • Regulatory challenges to overcome for CE marking CDx

Keywords: In vitro diagnostic medical device (IVD), companion diagnostic (CDx), IVD regulation, CE marking, EU IVD regulatory framework, Notified bodies

About the presenters:

Sylvie Le Glédic is the Director, Medical Devices & IVD at VCLS. She is actively involved in the evolution of the EU IVD and MD regulations, and closely follows the new rules for regulatory approval of Companion Diagnostics (CDx), both in EU and US.

About VCLS:

VCLS supports life science companies and engages in communication with regulators and payers to develop, register and launch innovative health products in global markets.