Medical Devices (BYRD Health):

Navigating Product Compliance in Healthcare

March 27, 2025

Loksite Mannheim

English

Your Gateway to Master Data Excellence in UDI

The medical device industry faces increasingly complex regulatory challenges, from UDI compliance and EUDAMED registration to global reporting obligations. At the same time, sustainability requirements are growing, with greater emphasis on traceability, digital compliance, and eco-friendly procurement. But how can MedTech companies efficiently navigate these evolving requirements while maintaining competitiveness?

Our Medical Device Event offers practical insights and concrete solutions to not only meet compliance requirements such as UDI, MDR, and EUDAMED, but also to leverage them strategically for operational efficiency and market leadership.

Agenda

  • 9:30 – Get Together & Networking
  • 10:00 – Welcome
  • 10:15 – European Commission Regulation Update
    Meinrad Kempf, Medical Mountains
    Overview of the latest regulatory developments impacting medical devices in the EU and beyond, including MDR, UDI, and compliance strategies
  • 10:45 – HCDP Track 1
    Jens Kalecinski, Head of Product Data Management, Prospitalia

    Exploring digital platforms for product data management, optimizing purchasing processes, and ensuring regulatory compliance.
  • 11:15 – Live Demo: Digital Compliance for Medical Devices
    Thomas Mertens, Healthcare Consultant, BYRD Health

    Guest Speaker: Representative from Pajunk
    Step-by-step guide to fulfilling EU MDR UDI requirements, data submission to EUDAMED, and best practices for compliance.
  • 12:00 – Lunch & Networking Break
  • 14:00 – BYRD Health User Group: Vigilance & Compliance
    Lionel Tussau, BYRD Health
    Updates on vigilance reporting, UDI registration, and global regulatory frameworks with insights from industry experts.
  • 15:00 – Status Quo on Healthcare Plus Eco
    Speakers from GS1 Netherlands & GS1 Denmark
    Discussion on sustainability initiatives in healthcare, including eco-friendly procurement and digital traceability.
  • 15:30 – Coffee Break & Networking
  • 15:45 – Staying Ahead of the Curve: Global UDI Compliance & Registration Strategies
    Jay Crowley, Vice President, USDM Life Sciences
    Jeff Holzman, Lead Amercias and Strategy, BYRD Health
    Best practices for UDI compliance, upcoming deadlines, and evolving global regulatory requirements.
  • 16:30 – Summary of the Day
  • 16:45 – Afterwork Networking

Secure your place and gain practical knowledge, valuable insights from leading experts, and the opportunity to exchange ideas with other professionals in the MedTech industry. Learn how to efficiently navigate UDI compliance, EUDAMED registration, and sustainability requirements—ensuring compliance with minimal effort and maximum benefit.

We look forward to welcoming you to the Medical Device Event in Mannheim!

Getting there and parking:

Mannheim Central Station is only about a 10-minute walk away. If you are traveling by car, the following parking options are available:

We recommend looking for a parking space early, especially at peak times.

Register now

Our Keynote Speaker
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Henning Jaeger

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Jay Crowley

Vice President
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Lional Tussau

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Thomas Mertens

Healthcare Consultant
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Meinrad Kempf

Projektmanager
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