OCRA-DG Conference 2026

Meet SGS at the 32nd Annual OCRA-DG Conference

Regulatory requirements continue to evolve, and bringing a medical device to market means managing compliance, quality, testing, and market access at every stage.

As a Gold Sponsor of the 32nd Annual OCRA-DG Conference, SGS will join regulatory affairs, medical device, biotechnology, and pharmaceutical professionals on September 2, 2026, at the Beckman Center in Irvine, California. Meet our specialists throughout the event to discuss regulatory challenges and practical ways to move products forward while maintaining quality, safety, and compliance.

Navigate Medical Device Compliance with SGS

Whether you are preparing documentation, addressing testing requirements, pursuing certification, or planning access to international markets, SGS can support your team across the medical device product lifecycle.

• Navigate IVDR Requirements: Discuss product risk classification, conformity assessment routes, technical documentation, and certification requirements for Class A sterile, B, and C IVDs.
• Prepare for Global Market Access: Explore regulatory and conformity assessment support for CE marking, UKCA, MDSAP certification, and other market requirements.
• Put Product Safety to the Test: Learn about testing capabilities for in vitro diagnostics, imaging equipment, active and implantable medical devices, medical PPE, packaging, and other medical technologies.
• Address Product Integrity Risks: Explore Container Closure Integrity Testing and Extractables & Leachables Testing for packaging integrity, sterility, material risks, and product safety.
• Strengthen Regulatory Knowledge: Discuss medical device training covering MDR, IVDR, and ISO 13485 requirements for regulatory and quality 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.

The conference concludes with a networking happy hour from 5:00 p.m. to 6:00 p.m., providing another opportunity to connect and continue the day's conversations.

Join SGS at the 32nd Annual OCRA-DG Conference and bring your regulatory, testing, certification, and market access questions to our specialists.

For further information, please contact:

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