11:30 am EST | 4:30 pm GMT | 8:30 am PST | 30 minutes
Part 1 of our series looked at how eConsent streamlines the consent process to be faster and yet increase patient comprehension. 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. Medrio’s ePRO and MyMedrio work together so you can:
The earlier you plan for and integrate technology such as ePRO and eConsent for your trials, the greater the efficiencies achieved. Let us start that journey to higher quality data and reporting compliance together.
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Date: Tuesday, March 22, 2022 Time: 11:30am - 12:00pm
This is a virtual event.