Teams running wearable studies finally have a sub-$100, screenless, all-day tracker option, and here is what the new Google Fitbit Air means for clinical research, from its sensors and accuracy to data export via the Google Health API.

eCOA validation actually covers four separate jobs: linguistic, equivalence, system, and psychometric. Here is what each one means, who owns it, and what FDA, EMA, ICH and TGA expect to see.

Real world data in clinical trials explained: sources, regulatory context, use cases, and a practical guide to capturing RWD in your next study.

Learn how eConsent works in clinical trials, FDA and 21 CFR Part 11 requirements, benefits over paper, and how to roll out electronic informed consent.

A signed consent form isn't the same as informed consent, and most eConsent platforms miss that distinction. Here are 10 best practices for designing eConsent.