MEDevice Boston 2026

SGS will be at MEDevice Boston 2026, August 26-27 at the Thomas Michael Menino Convention & Exhibition Center in Boston, Massachusetts. Visit us at Booth 529 to connect with SGS specialists and discuss medical device regulatory compliance, testing, certification, quality, and global market access.

The event brings together professionals across the MedTech sector, including engineering, research and development, manufacturing, regulatory and compliance, procurement, project management, and operations. SGS will be available to discuss how manufacturers can address regulatory requirements while supporting product quality, safety, and market readiness.

Supporting Medical Device Compliance and Market Access

SGS supports medical device manufacturers across the product lifecycle, with services addressing regulatory assessments, testing, certification, and compliance. Key areas include:

• IVDR Compliance: Support for EU In Vitro Diagnostic Medical Device Regulation (IVDR) requirements, including product risk classification, conformity assessment routes, technical documentation, and certification for Class A sterile, B, and C in vitro diagnostic devices.
• Medical Device Testing: Testing services supporting the safety, performance, quality, and regulatory compliance of medical devices, including active and implantable devices, imaging equipment, medical PPE, packaging, and in vitro diagnostics.
• Product Integrity: Container Closure Integrity Testing and Extractables & Leachables Testing to address sterility, packaging integrity, material risks, and product safety.
• Quality and Regulatory Training: Medical device training covering MDR, IVDR, and ISO 13485 requirements for teams responsible for regulatory compliance and quality management.
• Global Market Access: Regulatory knowledge and conformity assessment services supporting requirements including CE marking, UKCA, MDSAP certification, and international market approvals.

Medical Device Expertise from SGS

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.

Visit Booth 529 at MEDevice Boston 2026 to meet our team and discuss how SGS can support your medical devices with testing, certification, regulatory compliance, and access to global markets.