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Excipient World Conference & Expo 2026

  • Location

    Nashville, Tennessee, United States

  • Start

    May 04, 2026

    5:00 PM

  • End

    May 06, 2026

    3:00 PM

  • Time Zone

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

Meet SGS at Excipient World Conference & Expo 2026

SGS will be exhibiting May 4–6, 2026 at the Gaylord Opryland Resort & Convention Center in Nashville, TN. Visit us at Booth 407 to connect with our pharmaceutical and excipient compliance specialists.

SGS supports excipient manufacturers, API producers, and finished product organizations with independent audits, gap assessments, and certification aligned to global GMP and GDP expectations. Our services help strengthen supplier qualification, reduce redundant audits, and support regulatory confidence across the pharmaceutical supply chain.

How SGS Supports Excipient and Pharmaceutical Compliance

  • ICH Q7 Audits: GMP audits for API manufacturers covering facilities, materials management, production controls, validation, and distribution.
  • EXCiPACT Certification: Independent third-party GMP/GDP/GWP certification for excipients and pharmaceutical auxiliary materials to reduce duplicate customer audits.
  • 21 CFR Parts 210/211: U.S. FDA GMP audits for finished pharmaceuticals and OTC products.
  • ISO 15378: GMP and quality management integration for primary packaging materials in contact with medicinal products.
  • 21 CFR Part 111 / SSCI: cGMP certification pathways for dietary supplements and retailer acceptance requirements.
  • WHO GDP / WHO GMP: Distribution, warehousing, and secondary packaging compliance to maintain product integrity.
  • Integrated Audits: Combined multi-standard programs to streamline oversight and reduce disruption.

Special Session

Join Jon Gawlak, SGS North America, on Tuesday, May 05, 2026 from 11:15 AM – 11:35 AM CDT at Ryman Hall Stage 1 for the session:

“Supply Chain”

This presentation will examine how third-party excipient GMP/GDP certification programs such as EXCiPACT can support more efficient quality management across the pharmaceutical supply chain. The session will address audit costs, industry challenges, and how standardized certification frameworks can reduce redundancy while maintaining robust supplier qualification and compliance practices.

We look forward to connecting with quality, regulatory, technical services, and procurement professionals at Booth 407 to discuss practical approaches to excipient and pharmaceutical compliance.

For further information, please contact:

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

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