We can design a ‘roadmap’ or non-clinical development plan that outlines the minimal required non-clinical studies including timelines, costs, and risks.

Working in conjunction with other disciplines like CMC, clinical, and regulatory helps to ensure that your non-clinical program is fully integrated. For example, our non-clinical and clinical team of experts work hand in hand to ensure a rapid and smooth transition from safety testing to first-in-human trials.

Get in touch
with our Xpert

François van Och

Managing Partner, Non-Clinical Team Lead