08.06.26 -- Starting Material Importance

Effective CCIT goes beyond micron claims, focusing instead on repeatability, confidence, and real‑world relevance. Learn how to define a defensible LOD and understand what auditors truly prioritize.

Explore how traditional and innovative pharmaceutical packaging formats improve patient adherence, support emerging therapies, and shape the future of drug delivery and treatment outcomes.

Discover how our on-body delivery system supports high-volume biologic delivery by balancing usability, patient needs, and sustainability through research-driven design.

Viewing the Annex 1 revision as a natural extension, rather than a burden, allowed for a seamless transition. Since contamination control was already standard, the update simply validated existing excellence.

In this segment from the Pharmaceutical Online Live event, “Analytical Strategies for High-Volume GLP-1 Manufacturing” our panelists talk about the element of GLP-1 manufacturing received the least attention but is the most important operationally—the starting material.

Anmaris Torres, Process Engineering Team Leader, on why a process transfer starts with a conversation across departments to figure out how to cut cycle time before commercial production begins.