Speaker: Bill Neumann, VP Quality Assurance & Regulatory Affairs
Date: January 30, 2026
Analytical, Clinical
Pharmaceuticals & OTC
Bill Neumann reviews the OTC monograph system, critical steps to launching in compliance with FDA regulations, as well as company’s requirements when working with contract manufacturers.
Dr. Mike Traudt, PhD., leads a deep dive into the science of “bulletproof” claims. This session isn’t just about following rules; it’s about understanding the legal and regulatory challenges to ensure your brand builds, and keeps, consumer trust.
Plastic Container Testing for Drug Products with Implications for Cosmetics
Bill Neumann provides a comprehensive overview of the new USP and for plastic container testing that took effect December 1st, 2025. The presentation covers the importance of verifying plastic suitability for drug product packaging and identifying extractable materials that could migrate into products.
