Our Services
Dossier compilation, lifecycle management, authority liaison and scientific studies.
We build and format dossiers in line with national guidance, including REF/HP/05/14 in Morocco. The formulated-product package covers identity, physicochemical and technical properties, toxicology, analytical methods, application data, efficacy, selectivity, classification and labelling. The active-substance package covers identity, properties, analytical methods, toxicology, metabolism, residues, environmental fate, ecotoxicology and classification.
We manage renewals, regulatory surveillance, use and portfolio extensions, multi-brand strategies, dose and PHI changes, revised conditions of use, ownership transfers and supplier updates.
We perform completeness checks, organize submission, prepare responses to additional-information requests, update documentation and manage administrative follow-up through final validation and publication.
We coordinate with accredited GEP/GLP organizations for sample importation, field application, data collection, statistical analysis and extrapolation. We cover efficacy and selectivity trials, residue studies for MRL and PHI validation, and physicochemical, toxicological and ecotoxicological studies involving bees, birds, aquatic organisms and other non-target species.
Field observation and scoring
Leaf-mounted traps and observation supports help monitor pest presence, compare trial treatments and produce traceable evidence for GEP study reports.
