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6th Qserve MedTech Conference - Global Registrations

12 November 2026, Amsterdam. Three sessions: the PRRC role, building a regulatory intelligence system and putting EUDAMED to practical use. 

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PMCF Studies

 

The Global Registrations track brings together Qserve's global market access experts, Notified Bodies, and industry speakers for three sessions in a single day, covering the roles and systems that keep devices compliant across markets.

The day opens with the PRRC role — the responsibilities, challenges, and ethical questions that come with the position — before moving to regulatory intelligence, on building a system to track changing requirements without getting overwhelmed. It closes with EUDAMED, and a practical look at bulk upload and how to put its modules to use.

Amsterdam, 12 November 2026.

Who this track is for

This track is built for anyone managing regulatory compliance across markets or systems, not just within a single submission.

  • PRRCs and those stepping into the role, looking for clarity on responsibilities and the ethical grey areas that come with it

  • Regulatory affairs professionals building or maintaining a regulatory intelligence process
  • Compliance and QA teams working with EUDAMED, including bulk upload and day-to-day use of its modules
  • Global market access teams tracking how PRRC duties, regulatory intelligence, and EUDAMED fit together operationally

Sessions: Global Registrations

Three 90-minute sessions across 11 and 12 November 2026

  1. Session 1 Day 1 · 11 Nov · 11:00–12:30

    The PRRC Role: Responsibilities, Challenges & Ethics

    The Person Responsible for Regulatory Compliance (PRRC) plays a critical role under MDR and IVDR. This session explores responsibilities, challenges, and ethical considerations.

    Speakers

    • René Schings, Quality and Auditing Expert, Principal Consultant Qserve

  2. Session 2 Day 1 · 11 Nov · 14:00–15:30

    Regulatory Intelligence: Staying Ahead Without Overload

    Regulatory information is constantly evolving. This session helps you build an efficient regulatory intelligence system without getting overwhelmed.

    Speakers

    • Dennis Sarwin, Team Manager Global Registrations & Consultant Qserve
    • Adelina Chiaravalloti, Director, Regulatory Affairs and Clinical Evaluation Corcym

  3. Session 3 Day 2 · 12 Nov · 14:00–15:30

    EUDAMED Bulk Upload: Practical Use and Implementation

    EUDAMED is becoming central to EU regulatory compliance. This session provides a practical overview of its modules and how to use them effectively.

    Speakers

    • Dennis Sarwin, Team Manager Global Registrations & Consultant Qserve
    • Adelina Chiaravalloti, Director, Regulatory Affairs and Clinical Evaluation Corcym
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Qserve MedTech Conference

Choose Your Conference Experience

Pre-Conference Workshop Ticket

Join our hands-on pre-conference workshops on 10 November 2026 and gain practical insights through focused sessions designed to prepare you for the latest MedTech regulatory challenges.

€899,-

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Conference Ticket

Attend the two-day conference on 11 and 12 November 2026 to access expert-led sessions, industry insights, and valuable networking with MedTech professionals.

€1299,-

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Full Conference Ticket

Get the complete experience with access to both the pre-conference workshops on 10 November and the full two-day conference on 11 and 12 November 2026.

€1599,-

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We offer group tickets and special offers, contact training@qservegroup.com for more information.

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Global Registrations Track

 Qserve Speakers Global Registrations Track 

Dennis Sarwin, MSc

Team Manager Global Registrations & Consultant

René Schings

Quality and Auditing Expert

Principal Consultant