06/17/2026
When someone has trained hundreds of professionals over the course of a career, patterns begin to emerge.
The same mistakes. The same misconceptions. The same questions that surface whenever HPLC testing intersects with GMP requirements.
Not because people lack technical ability, but because regulated analytical testing demands more than technical knowledge. It requires an understanding of where science, compliance, documentation, and professional judgment meet.
This webinar explores the practical application of HPLC in GMP environments, including system suitability, mobile phase preparation, column selection, documentation requirements, peak integration challenges, common testing applications, and the effective use of Empower 3 software.
Drawing on decades of experience in pharmaceutical Quality Control, Stability, Method Transfer, Analytical R&D, and Operational Excellence, Kevin Mueller brings a perspective shaped not only by regulations, but by years spent helping professionals navigate them successfully.
The goal is simple: to better understand what GMP allows, what it does not, and why that distinction matters.
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