The experts at Nelson Laboratories have been busy in 2017. They have participated on committees, spoken at domestic and international industry events, written whitepapers, published articles, and hosted webinars. We have compiled the list below to share some of our educational assets:
- Medical Device Disinfection for Reprocessing Products for US and EU
- Developing a Biological Safety Evaluation
- Considerations for Third-Party Reprocessing of Single-Use Medical Devices
THIRD-PARTY PUBLISHED ARTICLES
- Single-use medical devices: Here’s how reprocessing is possible
- Is Your Biocompatibility Program on the Edge?
- Reusable Devices: How Effective Is Your Cleaning Validation?
- New Expectations for Biocompatibility Testing: Are You Ready?
- Extractable/Leachable Chemistry Testing Strategies for Medical Device
- Part of the Process
- Great Expectations
- Testing Your Patience
- Let’s Keep it Clean, Folks
- US FDA guidance on the use of ISO 10993-1 for the biological evaluation of medical devices: the top 10 changes affecting medical device manufacturers
To register for our three-day Science of Sterilization Validation seminar, visit the Seminar page on our website.