Informed consent to participation in a clinical trial involves substantially more than obtaining signatures from subjects on a written form. It includes providing to potential participants enough information… Read more

A common trend in the drug development industry is to utilize data and innovation to safely begin participant involvement earlier and earlier in clinical trials.  As innovation continues… Read more

Let’s talk adaptive trial design, particularly as it pertains to early clinical research right now.  Both large and small pharmaceutical companies see the potential to shorten development timelines… Read more