Implementation and compliance with national or international chemical or product legislation;

Toxicological safety assessment of substances and products;

Human health exposure and risk assessment;

Biocompatibility assessment;

Preparation of registration dossiers;

In silico modelling, i.e., prediction of toxicity by (Quantitative) structure-activity relationship ((Q)SAR) trend-analysis and read-across using software tools OECD QSAR Toolbox, Toxtree, Toxmatch, Vega etc.;

Exposure modelling by ConsExpo, ECETOC TRA, SprayExpo, RISKOFDERM;

Literature search;

Data gap analysis;

Advice on testing (development of integrated testing strategies, set-up of test designs);

Study monitoring;

Support by classification and labelling;

Evaluation of endocrine disruptive properties;

Assistance by development of novel or intelligent products/materials or compositional substances;

Preparation of expert statements including judicial expertise and opinion.