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ON-DEMAND WEBINAR

EPA Regulatory and Testing Guidelines for Residual Efficacy: How to Make Antimicrobial Product Claims

Published Date: December 20, 2022

With the recent implementation of the EPA guidance for residual efficacy claims for antimicrobial products, there is a lot to understand when looking to make a claim for a residual sanitizing test substance.

This webinar provides a top-down summary of what each of these methods is intended to accomplish and which method(s) may be the best fit for your test substance. Specifically, the webinar provides insight into how the results of a residual-efficacy evaluation for submission to the EPA can best be gathered, interpreted, and presented for the sponsor’s submission.

Learn more about the presenter below.

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Grady Wertman

Study Director

Grady Wertman is an experienced microbiologist and study director with extensive background supporting sterility assurance and microbiological testing programs for medical device and pharmaceutical manufacturers. Grady is recognized for his strong technical foundation and detailed understanding of test methodologies, with a focus on ensuring studies are designed, executed, and documented to meet regulatory and client expectations. He holds undergraduate degrees in Cellular Biology/Neuroscience and Microbiology from Montana State University.

Complete the form below to access the webinar.