Build a multi-page consent walkthrough tailored to the specifics of the study and participants. Provide accurate and tailored consents form based on site, rules, or patient demographics.
Engage with participants by letting them know they have a new consent to consider. Make sure participants always get the last version.
IRBs, sites, and sponsors collaborate in a single system—review real-time consent drafting progress and performance metrics.
Zapclinica helps you managing your clinical trial, reduces the time to market, the cost, and the burden to run a successful clinical trial by operationally streamlining every task in an all-in-one platform.