Analytical Method Validation Whitepaper
Analytical Method Validation White Paper Abstract
When validating analytical methods for Federal Insecticide, Fungicide and Rodenticide Act (FIFRA), it is important to understand the guidelines and their specific requirements. Under FIFRA, antimicrobial products designed to protect public health in the United States must be registered with the EPA to provide toxicology data, antimicrobial efficacy data and product chemistry data designed to support the purported label claims.
There are eight recommended parameters that should be included. In the whitepaper below, it will go into detail about each of the eight and why they are important in analytical method validation.
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Element offers a diverse, comprehensive suite of customized testing solutions and products for clients in the Antimicrobial, Food Production, Medical Device and Pharmaceutical industries.
Analytical Chemistry Testing
We offer our clients full product and analytical chemistry solutions. Our GLP and cGMP chemistry offerings include chemical characterization of active ingredients, testing of product-specific impurities, physical chemistry analysis and storage stability testing.
With more than 30 years of experience, we are the premier contract antimicrobial testing laboratory and expert partner to the developers, manufacturers and users of antimicrobial pesticide and biocide products.
Element offers a diverse array of microbiology testing services and can serve clients from early-stage antimicrobial product development and non-GLP screen testing all the way through GLP testing for submission.
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