CONSULTANCY

I can provide consultancy services across a wide range of disease areas, and from early stage planning to HTA submission.

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With over 12 years of experience across in vitro, in vivo and clinical research settings, I can also help plan & design methodologically robust pre-clinical or clinical research studies that are transparent, reproducible and at low risk of bias.

 

This typically includes items such as: study pre-registration; study protocols; research questions; positive and negative controls; minimum sample sizes; & robust analysis methods.