MEDICA 2025

SGS North America at MEDICA 2025

Hall 9, Booth B23 | November 17–20, 2025 | Messe Düsseldorf, Germany

Join SGS North America at MEDICA 2025, one of the world’s leading trade fairs for medical technology, diagnostics, and healthcare innovation. Meet our experts in Hall 9, Booth B23 to learn how SGS helps manufacturers navigate complex regulatory landscapes, ensure product safety, and achieve market access efficiently.

What You’ll Find at Our Booth

Our team will share insights and guidance on:

• IVDR Compliance and CE Marking – Understanding conformity assessment routes and documentation for Class A sterile, B, and C in vitro diagnostic devices.
• MDR, UKCA, and Global Approvals – Meeting multi-market regulatory requirements with precision.
• Software as a Medical Device (SaMD) – Certification and evaluation for software-based medical technologies.
• Testing and Auditing Solutions – Including container closure integrity testing, extractables and leachables analysis, and unannounced audits.
• Training and Compliance Programs – Covering MDR, IVDR, ISO 13485, and other critical standards.

Your Partner for Global Compliance

At SGS, we help bring medical devices to market safely and efficiently. As a full-solution provider, we help medical device clients ensure their products are of highest and consistent quality, while meeting the regulatory requirements for their intended purpose. We offer medical device CE marking as a Notified Body through our affiliate in Belgium (1639) for clients needing certification specifically for Software as a Medical Device (SaMD) products. SGS is a UK Approved Body (0120) able to provide conformity assessments under the UKCA scheme for Great Britain and is an Auditing Organization (AO) for MDSAP certification. SGS provides training, assessment, testing and certification through our network of more than 2,700 offices and laboratories across the world.

Connect with SGS North America at MEDICA

Our regulatory and technical specialists will be available to discuss how SGS North America supports medical device innovation and compliance through testing, certification, and training. Visit Hall 9, Booth B23 to learn how our global expertise and local insight can help you meet the highest standards of safety, performance, and quality.

For further information, please contact:

Dominic James
Marketing Assistant
t: +1-862-339-6737