Topic Sterility Assurance With Noelle Clifford

Sterility assurance in pharmaceutical manufacturing is complex, demanding rigorous controls from raw materials to finished product. Expert Noelle Clifford addresses key challenges in this Q&A, debunking common misconceptions and outlining best practices. She emphasizes a robust program encompassing meticulous equipment management, controlled personnel and material flow, and comprehensive environmental monitoring.

Clifford highlights the critical role of environmental monitoring in evaluating cleanroom performance and advocates for proactive regulatory engagement. Facility design, she notes, significantly impacts sterility, requiring cross-functional collaboration for optimal contamination control.

Interested in building a robust sterility assurance program? Read the full article for deeper insights.