Education and automation for increased efficiency
Tackling the challenges of increased protocol complexity and delays in patient enrollment
Clinical trials continue to grow in complexity resulting in increased trial costs and impacting patient enrollment rates. Industry figures tell us that 68% of protocol deviations are related to study procedures and that one third of site inpspections are triggered due to a failure in compliance.
Reducing the risk without changing the complexity
You may not always be able to reduce protocol complexity but you can reduce the risk associated with compliance by providing clear procedures and training to optimise performance and increase predictability in your trial.
Education of key stakeholders and automation of a range of clinical trial activities will enable you to;
- Reduce the cost of trial management
- Improve data quality and reduce data variability
- Accelerate patient enrollment
- Increase site and study team satisfaction and enagement
Making it easier for the patient, site and study staff
The FIRECREST Study Portal, which is full customisable to your study, provides single sign-on to a range of education and automation solutions. Connectivity to key stakeholders leads to increased engagement and improved study performance. A flexible enterprise reporting solution offers actionable operational intelligence and management insights on demand, focused on driving value and giving the study team a greater opportunity to manage the study and detect emerging issues.
Training Site & Study Staff - Award winning, impactful and interactive content
Visit-by-Visit Guide - Comprehensive essential instructions for site and study staff
Patient Education - eConsent Viewer - enhanced informed consent
Pre-Screen - Supporting identification of potentially eligible patients for screening and transparency into process
TrialDrive - eDocument distribution, management and tracking
eConsent Signature - capturing biometric signatures
Deployment of FIRECREST onto your study can take as little as 6 weeks from kick off meeting.
Bringing benefits to your trial
Our clients are already seeing the benefits of FIRECREST, including increase in enterprise compliance, reduction in protocol deviations and costs associated with training and document management.
In a recent research (conducted by Fletcher Spaght Inc.) comparing trials with and without FIRECREST:
FIRECREST trials demonstrated on average 40% fewer protocol deviations per subject visit and were twice as fast to first patient screened and to randomise patients
Contact us today to find out more about our solutions and how you can improve timelines and compliance.
Study Portal Access and Customer Support
To login to the FIRECREST Study Portal or to contact Customer Support please use the below links: