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Advocacy
Agrochemical Product Analysis CEMAS is able to provide the full range of analytical data in support of product registration. The Section has over ten years' experience in the provision and reporting of experimental data for submission of Plant Protection Products ... [more]
Bioanalysis CEMAS provides a comprehensive bioanalytical service for samples collected during pre-clinical and clinical trials. This area of expertise allows us to provide full method development, transfer validation studies and capacity to accommodate easily large-scale samples analysis ... [more]
Biocides CEMAS is able to provide the full range of analytical data in support of biocide registration. The Section is experienced in the provision and reporting of experimental data for submission of studies undertaken to satisfy the data requirements for registration of Biocides products within the EU as outlined in directive 98/8/EC ... [more]
Ecotoxicology CEMAS carries out a range of studies to evaluate the aquatic and terrestrial ecotoxicological effects of substances, including plant protection products and active ingredients, industrial chemical products, effluents and waste-waters ... [more]
Efficacy Testing CEMAS is a GLP and GEP-compliant laboratory offering a range of laboratory-based studies for the generation of efficacy data in support of registration of plant protection products as required by Commission Directive 93/71/EEC ... [more]
Field Trials Field trials of agrochemicals are undertaken through our alliance partners in Europe and in North America. The field stations used are all GLP-compliant and provide access to a wide range of crops, targets and soil types in diverse environmental conditions ... [more]
Operator Exposure CEMAS have a dedicated team with staff experienced in carrying out OPEX studies worldwide since 1985. We are particularly experienced in Europe and recently completed studies in the UK, France, Spain and Portugal ... [more]
Pharmaceutical Analysis The Pharmaceutical Section undertakes work in compliance with GMP and GLP regarding pharmaceuticals and veterinary medicines ... [more]
Registration
Quality Assurance The QA Unit is independent of the Scientific Sections and is responsible for monitoring the planning, conduct and reporting of the studies and projects directed by CEMAS staff for compliance with Good Laboratory Practice and Good Manufacturing Practice regulations ... [more]
REACH Under the new EU system of Registration, Evaluation, Authorisation and Restriction of CHemicals (REACH), enterprises that manufacture or import more than one tonne of a chemical substance per year will be required to register it with the new European Chemicals Agency ... [more]
Residue Analysis The Residue Analysis Section analyses crop, soil and veterinary residues to generate data to support agrochemical and veterinary registration ... [more]
