Our preclinical toxicology offering supports assessment of test-article effects before later development decisions. The study should be designed around the intended exposure and program stage.

Provide the material, proposed administration and safety question; identify the quality and report requirements. Agree the test-article characterization, design rationale and assessment endpoints, including how the findings will inform the next decision.

CROaccess can help coordinate your preclinical toxicology enquiry through its free procurement support; we confirm the scope and quote for our work.

Request an introduction through CROaccess