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2025 Audit Division Conference

  • Location

    Reno, Nevada, United States

  • Start

    September 10, 2025

    7:30 AM

  • End

    September 11, 2025

    4:00 PM

  • Time Zone

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

Visit SGS at Table 9

Join us at the 2025 Audit Division Conference, September 10–11 at the Peppermill Resort Spa & Casino in Reno, NV. As a Diamond Sponsor, SGS will showcase its leadership in medical device auditing, testing, and certification.

Why Visit SGS at the Conference

  • IVDR and MDR Expertise: Engage with our regulatory specialists to understand the EU In Vitro Diagnostic Regulation, Medical Device Regulation, and market-specific pathways for compliance.
  • Conformity Assessment Support: Explore CE marking processes for IVDs under our designation as EU Notified Body (1639) in Belgium, with additional SaMD certification available through our Finland (0598) affiliate.
  • UKCA and MDSAP Guidance: Learn how SGS supports conformity assessments as a UK Approved Body (0120) and as an Auditing Organization (AO) under the Medical Device Single Audit Program.
  • Comprehensive Testing Services: Gain insights on container closure integrity, extractables and leachables, and certification for active, implantable, and software-driven devices.
  • Training and Knowledge Sharing: Discover how our specialized training programs on MDR, IVDR, and ISO 13485 can strengthen your compliance teams.

Don’t Miss Our Presentations

  • Medical Auditing Masterclass and The Current Realities and Future Potential for AI Application in Auditing presented by Balázs Bozsik, Business Assurance, Technical Director – Medical Audit, NAM
  • Common GMP Audit Findings presented by Jon Gawlak, Business Assurance, Technical Manager / Senior Auditor

Our Global Reach

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), and in Finland (0598) 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.

For further information, please contact:

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

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