CleanMed 2026

Meet SGS at CleanMed 2026

SGS will be onsite at CleanMed 2026, May 12–14 at St. Louis Union Station. Visit us at Table 6 to discuss medical device compliance, certification pathways, and strategies for responsible market access.

Advancing Compliance and Accountability in Medical Devices

Health care leaders are navigating increasing expectations around product safety, regulatory alignment, and long-term performance. SGS works with medical device manufacturers to support compliance with IVDR, MDR, UKCA, ISO 13485, and other global requirements through independent assessment, laboratory testing, and certification services.

Connect with our specialists to explore:

• IVDR conformity assessment and CE marking routes
• Classification and certification for Classes A sterile, B, and C devices
• Technical documentation expectations for self-testing devices
• Compliance considerations for Software as a Medical Device (SaMD)

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.

We look forward to meeting you at Table 6 to discuss how SGS can support your compliance priorities and broader sustainability objectives.

For further information, please contact:

Dominic James
Marketing Assistant
t: +1-201-508-3000