Andrew Thomas, Lab Manager at WESTPAK, presented about "Validated Testing for Medical Device Packaging" with topics including:

- Regulatory Requirements for Validation: EU: MDR, ISO 11607-1:2019; US: FDA, CFR Title 21
- Test Method Validation: Repeatability, Reproducibility; Recommended Test Inputs
- Validated Package Tests: Medical Devices & Accessories; Compliance Requirements

Andrew's presentation was part of a live webinar called "Balancing Data with Risk to Improve Patient Safety" which was hosted by DuPont™ Tyvek® Medical & Pharmaceutical Packaging on January 27, 2021.

Explore Andrew's bio and learn more about this full webinar here: [ Ссылка ]

Visit WESTPAK's website: [ Ссылка ]

Learn more about DuPont™ Tyvek® Medical & Pharmaceutical Packaging: [ Ссылка ]

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