A Deep Dive into E&L and Biocomp Testing
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In this Medtech Matters podcast episode, sponsored by Nelson Labs, we’re discussing the importance of E&L (extractables and leachables) and biocompatibility testing for a variety of medical devices. The pair from Nelson Labs—Audrey Turley, B.S., Director of Lab Operations – Biosafety, and Kristin Treece, Ph.D., Principal Scientist - Analytical Chemistry—bring their expertise to the conversation, where a number of issues are resolved. During this episode, the following questions are addressed:
- First, what is Nelson Labs? What do you do?
- What is E&L testing?
- Why is it important?
- What is being tested?
- Is this done on all medical devices?
- Are there different tests for E&L depending on the device and/or application?
- When is E&L testing performed?
- What is biocomp testing?
- Why is it important?
- When is it performed?
- How do you perform in vivo testing? (and what does in vivo mean?)
- Anything else device manufacturers need to know about E&L and/or biocomp testing?
Listen to this discussion and see if you still have questions about E&L and/or biocompatibility testing. If you do, reach out to Nelson Labs to get answers. Feel free to use the links or contact mechanism here.
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