Jul 31, 2020
There are three different
instructions for use that need to be considered when preparing a
medical device for sterilization: the sterilizer, the medical
device itself, and the packaging system. The FDA requires that
medical devices be tested in just one type of packaging
system and on this week’s release of the Beyond Clean Vendor
Spotlight Series, we speak with Barbara
Ann Harmer about the maze that is instructions for use to
help people understand which IFUs to use under which circumstances.
How do validation and user verification work together to help you
make the right decision and focus on best practices that result in
patient safety? If you've ever debated this issue in your
department, you're not going to want to miss this Vendor Spotlight
episode so tune in now!
by visiting www.onetray.com, e-mail them
at firstname.lastname@example.org and look for educational information
and ask questions directly
on LinkedIn and Facebook.
#InstructionsForUse #MedicalDevice #PackagingSystem #Sterilization
#Validation #Verification #ONETRAY #SterileProcessing #BeyondClean
#CS #MDR #SPS #Surgery