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Combination Products Summit 2026

  • Location

    Rhode Island, United States

  • Start

    May 27, 2026

    8:00 AM

  • End

    May 28, 2026

    2:00 PM

  • Time Zone

    Eastern Time (US & Canada) (-05:00)

Meet SGS at the Combination Products Summit 2026

SGS will be participating in the Combination Products Summit 2026, May 27 to 28, at the Providence Marriott Downtown in Providence, Rhode Island. Connect with SGS specialists to discuss regulatory compliance, certification strategies, and market readiness for combination products and connected healthcare technologies.

As regulatory expectations continue to evolve across global markets, SGS supports manufacturers with assessment, testing, certification, and compliance services designed to help streamline development while supporting product quality, safety, and performance.

Supporting Combination Product Compliance and Market Access

SGS supports organizations across the medical device and combination products sector through:

  • IVDR and MDR Support: Guidance on classification, conformity assessment routes, technical documentation, and regulatory expectations for global market access.
  • CE Marking and Certification: Support for Classes A sterile, B, and C devices through our affiliate in Belgium (1639).
  • UKCA and MDSAP Services: Conformity assessments under the UKCA scheme and MDSAP certification support.
  • SaMD Compliance: Regulatory evaluation and certification support for Software as a Medical Device applications.
  • Product Integrity Testing: Container Closure Integrity Testing and Extractables and Leachables Testing to support safety and effectiveness.
  • Medical Device Training: MDR, IVDR, and ISO 13485 training programs designed to strengthen compliance readiness and internal capabilities.

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 connecting with attendees seeking practical approaches to compliance, lifecycle management, and combination product development.

For further information, please contact:

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

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