RAPS Convergence 2026

Meet SGS at RAPS Convergence 2026

SGS will be at RAPS Convergence 2026, September 15 to 17 at the Charlotte Convention Center in Charlotte, North Carolina. Visit us at Booth 1018 to connect with SGS medical device specialists and discuss regulatory compliance, conformity assessment, testing, certification, and global market access.

For regulatory and quality professionals, bringing a medical device to market means navigating requirements that can vary by product, classification, and destination. SGS supports manufacturers in addressing these requirements while maintaining product quality, safety, and compliance throughout the product lifecycle.

Navigate Medical Device Regulation with SGS

Bring your regulatory questions to Booth 1018 and speak with our specialists about areas including:

• EU MDR and IVDR: Discuss regulatory requirements, product risk classification, conformity assessment routes, technical documentation, and certification, including IVDR requirements for Class A sterile, B, and C devices.
• CE Marking: Learn about conformity assessment and certification support for medical devices entering the European market, including Software as a Medical Device (SaMD).
• UKCA: Explore conformity assessment requirements for medical devices intended for the Great Britain market.
• MDSAP Certification: Discuss medical device quality management system auditing and SGS's role as an Auditing Organization (AO) for MDSAP certification.
• ISO 13485: Explore assessment, certification, and training supporting medical device quality management systems and regulatory requirements.
• Medical Device Testing: Discuss testing capabilities for in vitro diagnostics, imaging equipment, active and implantable medical devices, medical PPE, packaging, and other medical technologies.
• Product Integrity: Learn about Container Closure Integrity Testing and Extractables & Leachables Testing to address packaging integrity, sterility, material risks, and product safety.
• Regulatory Training: Explore training programs covering MDR, IVDR, ISO 13485, and other requirements relevant to medical device compliance teams.

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.

Whether you are working through a conformity assessment, preparing for certification, addressing testing requirements, or planning entry into another market, meet the SGS team at Booth 1018 to discuss the next steps for your medical device.

For further information, please contact:

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