Meet Qarad at one of the many conferences and fairs we attend!

Contact us to schedule a meeting at one of these events.

Upcoming events

Impact of IVDR on clinical drug trials within the EU

Our Regulatory Affairs Expert Anne Paulussen will tell you more about:

  • the new European IVD (In Vitro Diagnostic) regulation
  • how the new regulation applies to assays used in clinical (drug) trials
  • the current state of play for companion diagnostics in the EU
  • some of the challenges we are currently facing in this field

Regulatory Requirements, Technical Documentation, & Performance Evaluation for In-House Developed Tests

Our Device Compliance Senior Expert Pieter Bogaert will give you more information about:

  • regulatory aspects for assays used in clinical trials
  • understanding IVDR Article 5.5 for in-house developed tests
  • understanding IVDR Annex I General Safety & Performance Requirements
  • performance Evaluation of in-house developed tests

Previous events

Key elements to consider to successfully bring your Swiss IVDs to the EU market

A high-level overview of key elements to be taken into account under the IVDR in order to gain access to the EU market.


Meet with Qarad experts at MEDICA 2022 Düsseldorf (GERMANY) on 14-17 November ’22 MEDICA is the world’s largest event for the medical sector. For more than 40 years it has been firmly established on every expert’s calendar. Are you attending the fair? Let’s meet!

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