toxconsult offers additional services in all areas of toxicology aimed on optimizing a sustainable establishment of your safe products on the market. We provide technical support for the conduct, monitoring and evaluation of studies in-house or with CRO´s. Analysis of existing data, evaluation, interpretation, peer reviews, support concerning electronic data recording and storage as well as electronic transfer of registration documents are part of our management service. Our support includes designing and conducting studies to explain mechanisms for certain findings and relevance for humans. Furthermore we review and establish presentations or position papers regarding results, which are relevant for registrations or special scientific topics. On request we also offer presentations to authorities and attendance at meetings with authorities, conferences, etc. toxconsult provides support for all questions regarding quality assurance and good laboratory practice (GLP) as well as for conducting GLP training and other seminars on toxicology-related topics. We gladly assist you with our expertise in many areas of R&D besides toxicology and safety pharmacology, like international authorities´ registration requirements (EPA, FDA, PMRA, European authorities, JMAFF, etc.) for chemicals, agrochemicals, pharmaceuticals and animal health products
- Study designs, protocols and reviews
- Data management
- Mechanistic methods
- Presentations and position papers
- GLP management and training
- Expertise provision
