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RAPS Global Regulatory Strategy Conference 2026

  • Location

    Baltimore, Maryland, United States

  • Start

    March 05, 2026

    8:00 AM

  • End

    March 06, 2026

    4:00 PM

  • Time Zone

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

Meet SGS at the RAPS Global Regulatory Strategy Conference 2026

SGS will participate as a Gold Sponsor at the RAPS Global Regulatory Strategy Conference 2026. Visit us at Table 3 to connect with our regulatory specialists and discuss practical approaches to clinical evaluation and global compliance strategy.

Sponsored Presentation

Join our sponsored session, Making Your SOTA and Device Literature Search Count: The Expectation Values of the Notified Bodies on Literature Searches, on Thursday, March 5, 2026, from 1:15 PM to 1:40 PM East Coast USA Time.

Presented by Kevin Holochwost, Technical Director, Product Assessor, SGS North America, this session addresses a frequent system-wide failure mode in clinical evaluation: State of the art literature searches. With clinical evaluation representing a significant portion of notified body non-conformities, this presentation will focus on expectation values for literature searches and how to determine whether data identification, safety and performance objectives, and supporting evidence are sufficient and measurable.

How SGS Supports Medical Device Compliance

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 continuing the regulatory dialogue at Table 3.

For further information, please contact:

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

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