The process of biopesticide registrations is arduous. Applicants must have registered production facilities, years of documented safety studies and supporting toxicology reports for EPA to review as part of pre-submission considerations and formal reviews. Once approved, registrants are entirely responsible for their pesticide and pesticide labeling as required by Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and EPA regulations (40 CFR Part 152 and 169).
EAS Consulting Group assists clients with biopesticide applications and production facility registrations. Our team of experts include regulatory experts and toxicologists who can help with data analysis, facilitation of pre-submission meetings and preparation of submissions for FDA reviews.
Contact us to discuss your EPA application requirements and how EAS can assist you.