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With advances in changing modalities due to reduced capacity, the industry is challenged to shift their thinking not just to increase capacity but to reduce cycle times, make modality choices and modify sterility validations while keeping up with regulatory changes and maintaining device quality. This event brings together voices from sterilization stakeholders to define and build the future of this industry, for the benefit of the patients.
Explore developments in changing sterilization technologies, modality validation processes and impacts to device quality.
Discover the best practices and case studies on how to balance technologies with changing standards, calculate the dosage levels for changes to modality on device materials and packaging, and a lot more.
Take part in interactive sessions, case studies, panel discussions, and Q&A sessions at the event and learn about the latest trends and innovations in the sterilization technologies and modalities.
Get inspired by learning how to reduce cycle times, build capacity, and maintain device quality in the sterilization process and connect with successful leaders who have achieved excellence in sterilizing medical devices.
It's been more than 30 years since entrepreneur and Chairman of the Group, Marcus Evans, launched the first of his businesses.
Picarro is revolutionizing human understanding of global carbon, water and nitrogen cycles through scientific measurements.
SteriTek is a high-volume E-beam/X-ray contract sterilizer and R&D innovation center serving the medical device, biotech, pharmaceutical and other industries. Steri-Tek is ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as S
SteriTek is a high-volume E-beam/X-ray contract sterilizer and R&D innovation center serving the medical device, biotech, pharmaceutical and other industries. Steri-Tek is ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as State of California Medical Device and Drug Manufac
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