Clinical Trial Protocol
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Clinical Trial Protocol
We develop scientifically robust clinical trial protocols
Our scientists, biostatisticians and medical experts provide strategical and methodological advice based on strong evidence in order to help you plan coherent and robust studies, mitigate risk, optimize resources and make the best possible data-driven decisions.
Protocol optimization
We also analyze and review your own design and assumptions from a scientific, cultural, operational, and regulatory perspective in order to ensure that they are consistent with the objectives and endpoints of your study.
Our Medical Director, Dr Yves Donazzolo, is an active member of some prestigious Independent Clinical / Scientific advisory boards and has overseen thousands of development programmes.
We can help you with:
- Selection of clinical endpoints
- Protocol - writing and review
- Sample size calculation
- Literature search and review