Patient Recruitment, Onboarding and Engagement in Clinical Trials has never been easier before, PatienTrials, a Patient Centric Platform for Clinical Trials offers an unified collaborative platform for Sponsors and CROs to manage all centrally, while the participant information is auto directed to respective local sites for recruitment and onboarding. Improved compliance across all sites while empowering them to focus on what they do best, taking care of patients. PatienTrials captures high-quality patient generated data through proprietary solutions based on modern methods, and is poised to make a positive impact on overall drug development.
- 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