As part of toxicopathological tests carried out in accordance with OECD, REACH, CIPAC and ISO guidelines, we ensure comprehensive implementation of:

​

• Conducting single-center studies andMulti-Site

• Development of the Research Plan or its stage

• Providing precise guidelines for sample collection and storage

• Guaranteeing data integrity during research

• Meticulous supervision of research documentation in compliance with Good Laboratory Practice (GLP) guidelines

• Providing sampling materials

• Transport of samples in controlled environmental conditions

• Carrying out histopathological tests at the highest level

• Preparation of additional photographic documentation of histopathological preparations

• Toxic-pathological consultations regarding test results

• Performing peer review of microscopic assessments (peer review)

• Return transport of test and trial documentation to the Research Unit

• Preparation of the Final Report or Report on the Research Stage

• Archiving documentation and tests