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Cleaning Validations

May 19, 2016

Endoscope Sampling Kit Now Available

With their flexibility and complex components, endoscopes present unique cleaning and disinfecting challenges. Endoscope manufacturers, regulatory bodies, and healthcare facilities are increasingly concerned about the spread of communicable diseases, including clinically relevant microorganisms, on reprocessed medical devices. The concern over...

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March 10, 2016

Nelson Labs Experts Invited to Present at Joint Conference

Thor Rollins, consulting manager, and Audrey Turley, research scientist, have been invited to speak at the joint conference of the Association of Analytical Communities Southern California Section (AOAC SCS) and Food and Drug Agency (FDA) 2016 Spring Conference. Rollins and...

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March 13, 2015

Tissue Processing Equipment Validations: What You Need To Know

The following is a preview of the article Cleaning, Disinfection, and Sterilization Validations for Tissue Processing Equipment, featured in the February 2015 issue of MD&DI magazine, by Nelson Laboratories Senior Scientist Alpa Patel.                ...

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October 15, 2014

Nelson Laboratories Scientist Provides Clarification on Tissue Bank Cleaning Validations

Nelson Laboratories, Inc. Alpa Patel, senior scientist in healthcare reprocessing, presented at the annual American Association of Tissue Banks (AATB) meeting last month on the topic of Equipment Cleaning and Disinfection Validations, something she calls, “the tissue industry’s compliance challenge.”...

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May 15, 2014

Importance of Cleaning and Sterilization Validations, Even When they may Not be Required

Department Scientist-Healthcare Reprocessing I recently attended the 10th Annual FDA and Changing Paradigm for HCT/P Regulation Conference, with my colleague Wendy Wangsgard, Department Scientist, Bioburden. We presented topics of interest that have surfaced the validation realm, in addition to learning...

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