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Toxicology

 

Our commitment is to provide you, our valued customers, with a fast and reliable route to clinical phase I-II studies.

 

We offer you a wide range of toxicity and DMPK studies as well as other preclinical safety tests that are essential for your preclinical drug development programs. As our valued client, you maximally benefit from our long track record of designing large and specialized in vivo studies.

 

Quality and flexibility are key factors in our work. We work closely together with you and ensure that no regulatory studies are overlooked that are required for your IND filing. As a direct result, we will design and execute the most cost effective development strategies for your drug candidates.

 

 

PDF Download: QPS Toxicology Overview