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April 28, 2025 - May 30, 2025
Permit manufacturers to discuss contemporary challenges to design, supply, transportation, containerizing and packaging of devices while ensuring sustained production, product performance, and sterility assurance in the face of evolving rules and regulations. Attendees will walk away with strategies to plan for existing and future capacity constraints while adopting cost effective EO reduction strategies and alternative modalities such as X-Ray, E-Beam, Alternative Gases, and more. Furthermore, attendees will learn how to manage risk for process control, microbial contamination, and production impacts while maximizing the knowledge and leadership strengths of sterility and microbiology experts within their organizations.