The development of new chemical products and materials, also as components of medical devices, requires precise knowledge of their composition and their physico-chemical and toxicological properties. As a GLP-certified analytical laboratory, we can support you in the development and approval process through tests according to EC test methods or OECD test guidelines. We provide you with our broad analytical expertise paired with the latest analytical equipment including a wide variety of coupling techniques such as UPLC-MSMS, HPLC-MSMS, HPLC-DAD (UV, FL, RI), GC-MS and ICP-MS.
The safety investigations are carried out under GLP in accordance with the Chemicals Regulation of the European Communities (EC) No. 1907/2006 (REACH Regulation), which came into force on June 1, 2007. REACH stands for Registration, Evaluation, Authorization and Restriction of Chemicals, and stands for the registration, evaluation, approval and restriction of chemicals. In order to classify and label the substances to be assessed, the ordinance provides guideline for physico-chemical, toxicological and environmental toxicological studies.
We also carry out analyzes of physico-chemical properties and content determinations in the context of toxicity / ecotoxicity studies.
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You can find a detailed list of our methods here.