Date & Time
Starts
Nov 16, 2026 8:00am CET
Ends
Nov 19, 2026 5:00pm CET
Location
Dusseldorf, Germany (Europe)
Language
English
Join us at MEDICA 2026, one of the leading events for the life and health science segment, from Nov.16–19, 2026, in Dusseldorf, Germany.
Gain insights into safety, security, sustainability and software services UL Solutions offers to medical device manufacturers.
Experts from UL Solutions will be at MEDICA INNOVATION FORUM, Hall 11. Connect with us to learn about:
- Electrical safety testing and certification services
- Electromagnetic compatibility (EMC) and wireless compliance
- Cybersecurity for medical devices
- Solutions for Software as a Medical Device (SaMD)
- Medical device regulatory testing and certification
- Home healthcare medical equipment testing and certification
- Conformité Européenne (CE) marking for medical devices and in vitro diagnostic devices (IVDs)
Hear from UL Solutions experts at MEDICA 2026
We are also excited to invite you to our expert-led sessions on:
Tuesday, Nov. 17, 2026, 12:30 p.m.
AI in Healthcare: Navigating Safety and Regulatory Considerations from Innovation to Market
Speaker: Christian Hoffmann, Principal Engineer, Medical AI, UL Solutions
Wednesday, Nov. 18, 2026, 2 p.m.
Good Practice (GxP) Training in Medtech: A Changing Story
Speaker: Colleen Loconte, Director of Regulatory Lifecycle, ComplianceWire (Software), UL Solutions
Want to speak with us one-on-one? Prebook a meeting, and we will contact you to learn more about your needs. We look forward to seeing you at MEDICA 2026.
Service portfolio
Safety Testing and Certification services
The growing complexity of medical electrical devices requires more advanced testing and certification to evaluate compliance with safety and performance requirements. IEC 60601 is a widely accepted series of standards for the basic safety and essential performance of medical electrical equipment and systems. It is an important standard, and noncompliant equipment can pose a significant risk to patients.
Medical Device EMC Testing and Certification
In healthcare applications, electromagnetic incompatibility is not just a nuisance; it is potentially life-threatening. Most global regulatory bodies recognize a product cannot be safe and effective if it is not also compatible with its intended electromagnetic environment. Our comprehensive medical device electromagnetic compatibility (EMC) testing and certification services will help you to efficiently meet regulatory requirements and increase global market access.
Software as a Medical Device (SAMD)
With the increasing popularity of smart medical devices, the healthcare industry has entered an era surrounding the development of healthcare software and applications.Whether it is a health software/app that collects users' blood pressure, or remote control of medical equipment for diagnosis and treatment, they are included in the scope of health software. We can provide evaluation and certification services for SaMD and health software to key industry standards, helping demonstrate the safety and efficacy of these products.
Cybersecurity for Health and Life Sciences
Mitigating cybersecurity vulnerabilities that can pose serious risks to patient safety and privacy requires robust cybersecurity risk management processes and rigorous testing to protect connected products and systems. Our safety science expertise, rigorous testing and certification services, and a global team of experts empower customers to integrate cybersecurity across their medical product and software lifecycles.
Medical Device Regulatory Testing and Certification
UL Solutions offers medical device manufacturers with a complete offering of third-party regulatory approvals, product testing and certification, auditing, cybersecurity testing, usability testing and training to support compliance challenges.
Home Healthcare Medical Equipment Testing and Certification
Manufacturers of home healthcare equipment are increasingly focused on device comfort and ease-of-use features and apps that simplify operation for non-medical professionals, allowing patients to integrate healthcare monitoring and treatment plans into their existing routines. UL Solutions offers testing, inspection and certification services to help customers navigate compliance for medical electrical equipment and systems in a home healthcare environment.
CE Marking for Medical Devices and IVDs
To launch medical devices in the EU, manufacturers must demonstrate compliance with European regulatory requirements and obtain Conformité Européenne (CE) marking for their devices.
CE marking indicates that a product has met applicable European Union (EU) standards for safety, health and environmental protection. Additionally, two key regulatory requirements govern EU market access for medical devices.
Speakers
Christian Hoffmann
Colleen Loconte
Joaquin Gomez Serrano
Christian Hoffmann
Colleen Loconte
Join us!
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