We operate independently and unbiased, so we can efficiently support the CRO selection process.
We help you to define and describe your non-clinical development plan as well as related safety and efficacy endpoints to optimally support your regulatory and clinical strategies.
Working in conjunction with other disciplines like CMC, clinical, and regulatory helps to ensure that your non-clinical program is fully integrated.
Our global network consists of a broad spectrum of KOLs, research institutes and contract research organizations (CROs) with whom we collaborate(d) in the past and present. As we operate totally independent and unbiased, we can efficiently support the CRO selection process to make sure we identified the best partner to execute your non-clinical efficacy and safety studies.