OpenClinica

Live tracking and visibility into enrollment progress and metrics.

Real-time dashboards for enrollment tracking, query management, and site performance with customizable reports for stakeholder visibility.

Real-time monitoring of individual site performance metrics.

Automated alerts and reminders across consent, randomization, and participant communications.

Verify participant understanding of consent materials.

Multimedia-rich consent experiences with comprehension checks, automated notifications, and secure e-signatures—fully remote, in-person, or hybrid.

Digital signature capture for consent forms.

Choose individual modules and add more as needed based on specific study requirements.

Dashboard tracking and management of data queries and resolution.

Build studies in hours with drag-and-drop tools, templated CRFs, and real-time validation. Reduces data queries by 50%.

Immediate feedback on data quality during entry.

Centralized oversight for managing multiple studies across diverse therapeutic areas.

Guided setup from study design to site training.

Pull lab results, medications, and vitals directly from EHRs into EDC, saving coordinators hours and reducing transcription errors.

Mobile-friendly patient reporting with automated reminders and clean, flexible forms that increase compliance and reduce missing data.

Rich media options for consent and patient education materials.

Reach enrollment goals with precision-targeted outreach, smart pre-screening, and real-time analytics at 3-5x lower cost per conversion than traditional methods.

Intelligent participant pre-screening for recruitment module.

Experienced consultants handle technical details including CRF design, protocol review, and validation documentation.

Support for both blinded and unblinded randomization schemes.

Intuitive interface for building studies without technical expertise.

Templated Case Report Forms for faster study setup.

Track and manage randomization inventory and study supplies.

Rapid deployment of studies to sites and participants.

Simple to complex randomization schemes with blinded or unblinded access, inventory management, and automated notifications integrated with study data.

Support team available outside traditional business hours for sites, coordinators, and data managers.

Dedicated account manager for each client who knows their studies, team, and goals.

Ongoing support and optimization services after study launch.

On-demand training access for refreshers and training new team members.