The registration of medical devices may require their biological evaluation and, in some cases, it is necessary to evaluate their biocompatibility on the basis of either bibliographical data or preclinical studies. Based on the available toxicological information and the corresponding risk assessment, the safety profile of the product can be defined, and the health of the patient guaranteed. In Dalia we have a team of ERT toxicologists with extensive experience in the toxicological evaluation of medical products according to ISO 10993.

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