Research / Registries

Cloud-based, multi-site clinical trial administration and patient access

Connecting the dots
between patients and research

Visiontree for research & registries is a 21 CFR Part 11 compliant cloud-based, interoperable application for multi-site clinical trial management and patient access.

The Visiontree application provides a library of over 400 electronic patient and clinician reported outcomes assessments for ePRO and eCOA use. Visiontree allows you to manage decentralized clinical trials to bridge the gap between clinical research and clinical care.

Proven to deliver a high level of patient compliance, accuracy and validation, Visiontree provides data collection and curation with EHR interoperablity in semantic context of the patient health record for optimal multi-center research & registry management and reporting.

VTOC Research Mobile Devices
Research e-Forms
Research e-Forms
Clinical Trials Builder
Clinical Trials Builder
Compliance Manager
Compliance Manager

Outcomes Packages by Specialty

Visiontree provides standards-based ePRO, eCOA and customized solutions in these, and other, core domains.

Core Domains - Oncology
Oncology
Core Domains - Cardiology & Heart
Cardiology & Heart Surgery
Core Domains - Neurological & Spine Surgery
Neurological & Spine Surgery
Core Domains - Orthopaedic Surgery
Orthopaedic Surgery
Core Domains - Behavioral Health
Behavioral Health
Core Domains - Research & Registries
Research & Registries

Patient & Clinical Outcomes Data Collection & Reporting

Nimble and interoperable. The Visiontree Optimal Care™ (VTOC) cloud-based system allows providers to deliver improved quality and efficiency for patient care.

Efficient

Save time with cloud-based, paperless workflow for all clinical research and patient reported outcomes forms

Form compliance alerts for patients and research teams

Access to an extensive library (1,000+) of electronic, validated electronic patient reported outcomes assessments (ePRO)

Template and Timepoint Manager to build and manage your own research protocols

Accurate

Electronic patient reported outcomes data collection and reporting at specific timepoints

Research team and patient reminders by timepoint for high completion rates

Proven to increase patient reported outcomes data collection rate by 40%+ over paper

Template Manager allows for patients on multiple protocols, including separate treatment arms

Interoperable

Integration with legacy EHR and research systems including Medidata Rave®

Import Hub for data mapping of historical data and scheduled exports from EHR and disparate databases

Connectivity with all data interchange standards (HL7, Web services)

Multi-institutional participation with site-level access and Admin-level Aggregate data reporting

Interested?

For more information.