EO Sterilization At A Crossroads: Preparing For Stricter Residue Limits And Regulatory Shifts
Source: Eurofins Medical Device Services
While Ethylene Oxide (EO) is unmatched in its ability to sterilize heat- and moisture-sensitive products, the regulatory environment is changing rapidly. To address the health risks associated with EO, new standards are imposing stricter residue limits and demanding more rigorous safety evaluations.
Experts break down the "what" and the "how" of these changes. We guide you through the intersection of ISO 10993-7 and ISO 10993-17, ensuring your team is prepared for the next era of medical device safety.
This webinar covers:
- The "Why": Understanding the drivers behind regulatory shifts.
- The Impact: Navigating the practical hurdles of ISO 10993-7.
- The Solution: Leveraging ISO 11135 updates to minimize EO exposure.
- The Support: How Eurofins assists with niche, small-scale sterilization needs.
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