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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.

François van Och

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François van Och

Managing Partner, Non-Clinical Team Lead

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