A wide range of standards, USP tests, and FDA guidance documents provide test methods and acceptance criteria for particulate contamination in medical devices. In this webinar, Mark Bumiller will discuss solutions from Entegris to help meet these qualification requirements.
Speaker(s)
- Mark Bumiller | Technology Manager, AMH
A wide range of standards, USP tests, and FDA guidance documents provide test methods and acceptance criteria for particulate contamination in medical devices. In this webinar, Mark Bumiller will discuss solutions from Entegris to help meet these qualification requirements.
/content/microsite-live/lifesciences-live/en/home/about-us/events/particulate-contamination-in-medical-devices-and-single-use-systems-azo-network-webinar-11886On Demand Webinar
Particulate Contamination in Medical Devices and Single-Use Systems
Key topics will include:
- The importance of subvisible particulate testing of medical devices and single-use systems
- Why and how subvisible particulate testing of medical devices is performed using the single particle optical sizing (SPOS) technique
- Detailed results from infusion sets and enteral bags
- Particulate testing for Entegris single-use systems (SUS), including Aramus® bag assemblies
- Internal particulate testing protocol and results comparing Entegris with competitors' products