MedTech Conference 2026

Meet SGS at The MedTech Conference 2026

SGS will be exhibiting at The MedTech Conference 2026, October 18 to 21, in Boston, Massachusetts. Visit us at Booth 706 to connect with SGS specialists and discuss medical device regulatory compliance, testing, certification, and global market access.

As medical devices and digital health technologies continue to evolve, manufacturers face the challenge of bringing new products to market while meeting regulatory requirements for safety, quality, and performance. SGS supports medical device manufacturers throughout the product lifecycle, helping them navigate conformity assessments, strengthen quality systems, and address testing and certification requirements.

Navigate Medical Device Compliance with SGS

Whether you are developing a new device, preparing for certification, or managing regulatory requirements across multiple markets, our specialists can help you explore:

• EU MDR and IVDR Compliance: Discuss product risk classification, conformity assessment routes, technical documentation, and certification requirements, including IVDR requirements for Class A sterile, B, and C devices.
• Global Market Access: Explore CE marking, UKCA conformity assessments, MDSAP certification, and regulatory requirements for medical devices entering international markets.
• Medical Device Testing: Learn about testing capabilities for in vitro diagnostics, imaging equipment, active and implantable devices, medical PPE, packaging, and other medical technologies.
• Product Integrity: Explore Container Closure Integrity Testing and Extractables & Leachables Testing to help address packaging integrity, sterility, material risks, and product safety.
• Quality Management and Training: Discuss ISO 13485, quality management system assessments, and training covering MDR, IVDR, and other medical device regulatory requirements.

Exploring the Future of SaMD Lifecycle Management

As software becomes an increasingly important part of medical technology, managing product updates while maintaining regulatory compliance presents new challenges. SGS will address this topic during a Solutions Showcase presentation, "Beyond Change Control: Toward Adaptive SaMD Lifecycle Management."

Join Mingxiang Xu, Technical Director, SGS North America, on Monday, October 19, from 11:30 to 11:45 AM, at the Exhibit Level, Medtech Campus, Solutions Showcase.

The presentation will explore how manufacturers can move beyond traditional change control to manage software evolution throughout the product lifecycle. Topics include planning evidence proportionate to risk, anticipating software changes, and improving collaboration between engineering, quality, clinical, and regulatory teams while maintaining safety, effectiveness, and regulatory readiness.

Supporting Medical Device Quality and Market Access

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.

Whether you are addressing regulatory challenges, preparing for certification, or managing changes to medical device software, SGS can help you explore the next steps.

Visit Booth 706 at The MedTech Conference 2026 to meet our specialists, discuss your medical device compliance needs, and learn more about our testing, certification, and regulatory support services.

For further information, please contact:

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