89. ST98: New Guidelines for Manufacturer Cleaning Validation artwork
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89. ST98: New Guidelines for Manufacturer Cleaning Validation

  • E89
  • 17:31
  • March 23rd 2023

You may be familiar with ST79 (steam sterilization) and ST91 (flexible endoscopes), but have you heard about ST98: Cleaning validation for healthcare products?

AAMI veteran Ralph Basile guides through what the new guidelines state about how manufacturers should be testing their devices to ensure clean products for patients, and how these changes could make for better manufacturer IFU's for end users down the road.

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Medical device processing is critically important to the safety of patients everywhere. This podcast from Healthmark Industries is about answering questions and sharing knowledge related to sterile processing, endoscopy, infection prevention, biomedical engineering, leadership, and products. Have a question you would like answered on the show? Send it to our email address [email protected].


Meet the Host

Kevin Anderson avatar
Kevin Anderson
Clinical Education Specialist - Healthmark Industries

Kevin Anderson is a Clinical Education Coordinator for Healthmark Industries. He is a registered nurse (BSN) with multiple certifications including CNOR, CSSM, CRCST, CHL, CIS and CER.

Before joining Healthmark Industries, Kevin worked for 18 years in the acute care setting serving in various clinical and leadership capacities including clinical coordinator of general surgery, operating room manager and manager of sterile processing and endoscopy services. His sterile processing team was recognized with IAHCSMM’s Confidence Builder Award for their outstanding quality improvement in 2018.