Precision Med TRI-CON 2025

Join SGS at Booth 8 at Precision Med TRI-CON 2025 – March 11-13 in San Diego, CA

As a global leader in medical device compliance, SGS provides regulatory testing, certification, and market access support to help manufacturers navigate evolving global regulations.

What’s Happening at Our Booth?

• Regulatory Compliance & Certification – Learn how SGS supports MDR, IVDR, CE Marking, UKCA, and ISO 13485 compliance.
• Specialized Testing & Certification – Discover solutions for biocompatibility, sterilization, cybersecurity, and functional safety assessments.
• Medical Device Safety & Market Access – Explore SGS’s regulatory pathways for active and implantable medical devices, in vitro diagnostics, medical packaging, and SaMD (Software as a Medical Device).
• Expert Consultation – Engage with our regulatory specialists for insights into notified body approvals, certification processes, and risk mitigation strategies.

At SGS, we help bring medical devices to market safely and efficiently. We offer medical device CE marking as a Notified Body through our affiliate in Belgium (1639) and in Finland (0598) for SaMD certification. SGS is also a UK Approved Body (0120) and an Auditing Organization (AO) for MDSAP certification. With a global network of 2,700+ offices and laboratories, we provide training, assessment, testing, and certification worldwide.

Visit Booth 8 to discover how SGS can support your business with regulatory compliance, precision medicine advancements, and diagnostics market strategies.

For further information, please contact:

Dominic James
Marketing Assistant
t: +1-862-339-6737