With the recent implementation of the EPA guidance for residual efficacy claims on antimicrobial products, there is much to unpack and understand when looking to make a claim for a residual sanitizing test substance. This webinar aims to provide a comprehensive overview of the new guidance and offer practical insights into making successful residual efficacy claims.
The goal of this webinar is to provide a top-down summary of what each of the EPA-approved methods is intended to accomplish and which methods may be the best fit for your test substance. Participants will gain a clear understanding of the specific requirements and objectives of the various testing methods used to evaluate residual efficacy.
The webinar will also delve into the process of gathering and interpreting the results of a residual efficacy evaluation. Attendees will learn how to effectively collect and analyze data to meet EPA standards. This includes understanding the nuances of different testing methodologies and how to ensure that the test results accurately reflect the efficacy of the antimicrobial product.
Furthermore, the webinar will provide guidance on how to best present the results for submission to the EPA. Effective presentation of data is crucial for gaining approval, and this session will cover the key elements of a successful submission. Participants will learn how to compile their findings into a compelling and compliant report that meets all regulatory requirements.
By the end of this webinar, attendees will have a thorough understanding of the EPA guidance for residual efficacy claims and will be equipped with the knowledge to navigate the complexities of making such claims. This is essential for professionals involved in product development, regulatory affairs, and quality assurance within the antimicrobial product industry.
Join us to enhance your understanding of residual efficacy claims and learn how to ensure your antimicrobial products meet the latest EPA standards for residual efficacy.