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Radisson Grand Place

Jan 25, 2027 8:00 AM - Jan 27, 2027 4:00 PM

47 Rue du Fossé aux Loups, Brussels, Belgium

2027 Combination Products in the EU (presented by DIA and RAPS)

Overview

DIA and RAPS are excited to once again jointly produce 2027 Combination Products in the EU, a summit convening 26–27 January at the Radisson Grand Place in Brussels, Belgium. This highly-interactive event will unite key stakeholders across the field—including representatives from EMA, the European Commission, Notified Bodies, National Competent Authorities and Industry—to explore a coordinated drug and device approach to incentivise competitive innovation in Europe.

Throughout the summit, experts will exchange ideas via action-oriented working groups that stimulate ideation and innovation around designing solutions for pragmatic implementation.

Don’t forget to arrive early to join us for a special preconference workshop on 25 January focused on Introduction to Combination Products in the EU: Regulatory and Practical Insights (separate fee required).

Check the meeting web pages and registration details here

 

Participant Testimonial

An impressive initiative by the organizers to bring together all parties involved in in-vitro diagnostics and medical devices for decision-making, resulting in an exceptionally focused group. – Ana Trullas – European Medicines Agency

What you will learn

By exploring current challenges and opportunities to unite for better pathways forward, the programme will highlight critical topics such as:

  • The changing EU Regulatory Landscape
  • EU AI Act
  • COMBINE
  • Platform Technologies
  • Cybersecurity
  • Home-use and Self-administration
  • And so much more!

Program Committee

  • Gert  Bos, PhD, MSc
    Gert Bos, PhD, MSc Chief Scientific Oficer, Executive Director, Partner
    Qserve Group B.V., Netherlands
  • Christelle  Bouygues, PharmD
    Christelle Bouygues, PharmD Senior Regulatory Affairs Officer
    European Medicines Agency, Netherlands
  • Tim  Chesworth
    Tim Chesworth Senior Director Regulatory Affairs
    Novartis, United Kingdom
  • Andreas  Emmendoerffer, DrMed, PhD
    Andreas Emmendoerffer, DrMed, PhD Principal Regulatory Program Director - Device and Combination Products
    Roche Pharma LTD, Switzerland
  • Sabina  L. Hoekstra-van den Bosch
    Sabina L. Hoekstra-van den Bosch Global Director Regulatory Strategy
    TÜV SÜD Nederland B.V., Netherlands
  • Amanda  Matthews
    Amanda Matthews Senior Director, GCMC for Combination Products & Medical Devices
    Pfizer R&D UK, Ltd, United Kingdom
  • Thomas Wejs  Møller, MBA, MPA
    Thomas Wejs Møller, MBA, MPA Senior Director Global Regulatory Affairs - Devices, Combination Products, Digit
    Novo Nordisk, Denmark
  • Jonathan  Sutch, PhD
    Jonathan Sutch, PhD Principal Medicinal Technical Specialist
    BSI Group, United Kingdom
  • Sophie  Tabutin
    Sophie Tabutin EMEA Regulatory Affairs Leader
    W.L. Gore & Associates, France

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