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Agricultural pesticide consulting
Non-dietary risk assessment (RDC 998/2025)
Design, monitoring, and scientific evaluation of toxicological and ecotoxicological studies conducted by third-party laboratories.
Technical support in in vitro and in vivo strategies for conducting toxicological studies.
Additivity calculation for estimating the acute toxicity of formulated products according to GHS criteria.
Preparation of the Medical Information Table (Guide No. 12, dated 09/18/2019 - version 2)
Filling out the FLORA form and preparing DCIPA (RDC 950/2024 and RDC 1005/2025)
Analysis of regulatory opportunities for prioritizing products with lower toxicological impact according to (RDC 294/2019)
Preparation of a Technical Evaluation Report for the Company (PATE)
Assessment of the Toxicological Relevance of Impurities (RDC 1006/2025) and preparation of the Declaration of Toxicological Relevance (DRTI), with critical analysis of the available data.
Application of technical training and skills development.
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