Part 1 of our series looked at how eConsent strengthens your consent process to ensure better patient comprehension, adherence, and retention. Our experts Melissa and David are back to dig into ePRO and how you can set your study up to achieve as much as 97% compliance with patient reported outcomes.
The earlier you plan for and integrate technology such as ePRO and eConsent into your trials, the greater the efficiencies achieved. Let us support your journey to higher quality data and maintaining global compliance together.