Maree Beare is CEO of Clinials, an AI native Protocol Intelligence Platform that turns a finalised clinical trial protocol into the operational and patient facing documents sites, sponsors and CROs need to start a study. She came to the problem as a patient advocate, having navigated the clinical trial system from the outside before deciding the administrative barriers she saw were solvable with the right technology.

Manual content generation is the roadblock in every workflow for every stakeholder  Sites wait between six to 20 weeks, just to get the inputs they need from the sponsors or CRO’s, then Sites put in another 21+ hours of manual work per complex study to create the docs they need at the sites such as Interpreting the protocol: reading through the Schedule of Activities, footnotes, visit windows, eligibility criteria and procedures to work out what has to be captured at each visit.

Maree has a special interest in this amendment Magi@home session When the trial has  protocol amendments Clinials have you covered.  Instead of days redlining the protocol, our delta report shows what's changed and impacts in minutes.  Then regenerate the impacted materials