Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
ResearchGuru EDC is a comprehensive electronic data capture solution designed to facilitate various types of research studies, including clinical trials, observational studies, registries, and post-market analyses, all through a managed setup. The skilled ResearchGuru team specializes in the configuration and testing of study-specific electronic case report forms derived from validated questionnaires and protocols. Based on the specific needs of each study, these forms can incorporate features such as branching logic, mandatory fields, validation checks, calculations, participant consent, role-based access, audit trails, and electronic sign-off. Research teams can monitor key metrics such as recruitment rates, study completion, and data quality through intuitive dashboards, which also enable the generation of tables, figures, listings, and comprehensive statistical analyses from the collected data. Furthermore, data can be exported in a variety of formats, including Excel, CSV, R, Stata, and CDISC. This service is particularly beneficial for contract research organizations (CROs), universities, research teams, medical-device and digital-health companies, as well as research charities that require efficient EDC configuration and study assistance. Ultimately, ResearchGuru EDC enhances the research process by providing a robust and user-friendly platform that streamlines data collection and analysis.
Description
The integration of eCOA and digital technologies is paving the way for the future of clinical research, seamlessly connecting traditional methods with innovative, patient-centered approaches. Choose YPrime's eCOA solutions to not only obtain high-quality patient data but also to enhance the overall user experience for sponsors, investigator sites, and patients alike. By employing a flexible software development strategy, YPrime is able to swiftly tailor and adapt functionalities to meet specific study requirements within an impressive timeframe of 8 to 12 weeks. Our engaging and visual design process allows clients to review the system at various stages of development, ensuring they are informed before the system goes live. Additionally, our pre-validated and customizable authoring environment not only streamlines startup timelines but also accommodates post-production adjustments, such as changes to study protocols, making it an indispensable asset for clinical research. This commitment to agility and responsiveness positions YPrime as a leader in the evolving landscape of clinical trials.
API Access
Has API
No
API Access
Has API
No
Screenshots View All
No images available
Integrations
No details available.
Integrations
No details available.
Pricing Details
Pricing is quoted per study based on complexity, questionnaire length, required logic, number of users and sites, reporting requirements, support needs, and study duration.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
Yes
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
No
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
No
In Person
No
Vendor Details
Company Name
ResearchGuru
Founded
2021
Country
United Kingdom
Website
edcstat.com
Vendor Details
Company Name
YPrime
Founded
2006
Country
United States
Website
www.yprime.com/ecoa/
Product Features
Electronic Data Capture
Audit Trail
No
CRF Tracking
No
Data Entry
No
Data Verification
No
Distributed Capture
No
Document Imaging
No
Document Indexing
No
Forms Management
No
Remote Capture
No
Study Management
No
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
Yes
HIPAA Compliant
No
Monitoring
Yes
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No
Electronic Data Capture
Audit Trail
No
CRF Tracking
No
Data Entry
No
Data Verification
No
Distributed Capture
No
Document Imaging
No
Document Indexing
No
Forms Management
No
Remote Capture
No
Study Management
No