Patient recruitment, onboarding, and engagement in clinical trials have never been easier. PatienTrials, a patient-centric platform for clinical trials, provides Sponsors and CROs with a unified, collaborative platform to centrally manage the entire process, while automatically directing participant information to the appropriate local sites for recruitment and onboarding.
By streamlining workflows and improving compliance across sites, PatienTrials empowers local teams to focus on what they do best providing exceptional patient care. The platform also captures high-quality, patient-generated data through proprietary solutions built on modern methodologies, positioning PatienTrials to make a meaningful and positive impact on the overall drug development process.
- Sponsor and CRO Dashboards with study and site metrics
- Site selection/qualification/approval control for each study
- Rollout Central Patient Recruitment strategy through trials.me & other partner channels
- Manage Onboarding Patient experience with approved study specific workflows that can be pushed to selected sites
- Central configurable ePRO & eCOA study templates that can be pushed to selected sites
- Central study content repository to be shared with sites
- Central study support center for Sites to raise questions or concerns during recruitment and onboarding
- Auto-generated audit and compliance checks reports for review
- Generate Custom reports on the aggregated data across all sites for a specific study
Beta features:
- Central logistics coordination of study kits & dosage deliveries to sites (Beta)
- Ability to record IRB meetings & approval (Beta)
- Central IRB Content Approval process (Beta)
- Mobile Device Management (Beta)
New features
1. Site invitations
2. PI Invitations
Enhancements
1. eConsent dashboard
Service Portal