Greenlight Guru Clinical
4.3 out of 5 starsRatings and Reviews 0 Ratings
Ratings and Reviews 12 Ratings
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What is Mosio?
Mosio empowers research teams to enhance participant engagement, streamline communication, and gather data effectively through the widely used medium of text messaging. Our platform offers research teams the tools to interact more effectively with participants via mobile devices, integrating engaging elements and automated messaging features.
WHO CAN BENEFIT?
+ Sponsors of clinical trials in the pharmaceutical and biotech sectors
+ Cancer treatment facilities and organizations focused on clinical research
+ Studies funded by the National Institutes of Health (NIH)
+ Agencies dedicated to public health
+ Professionals such as clinical trial managers, directors, project managers, principal investigators, and coordinators, along with all research personnel involved in participant communication.
ADVANTAGES
+ Engaging medication reminders and alerts for compliance
+ Automation of the data collection process
+ Boost in participant engagement and adherence rates
+ SMS reminders for appointments to reduce no-show rates
+ Improved participant retention through automated check-ins, ensuring ongoing communication and support. Overall, Mosio serves as a vital tool for enhancing the efficiency of clinical research endeavors.
What is Greenlight Guru Clinical?
Medical device and diagnostics companies running clinical studies are often stuck configuring EDC software that was built for pharmaceutical trials and never designed around FDA, EU MDR, IVDR, or ISO 14155 requirements. Greenlight Guru Clinical solves that by being the only electronic data capture (EDC) system built from the ground up for medtech, so teams aren't reworking someone else's pharma template to fit a device study.
Designed exclusively for medtech, Greenlight Guru Clinical combines an easy to use clinical data platform with industry leading customer service, so teams generate reliable, compliant clinical data with confidence.
Get a single, validated platform covering the full lifecycle of a device or diagnostics study, including:
Electronic Data Collection and eCRF design, with GCP compliant structures and built in audit trails
ePRO/eCOA for patient and clinician reported outcomes, collected in person or remotely on any device
eConsent for compliant, auditable enrollment
Randomization (RTSM) for controlled and comparative studies
PMCF Surveys for post market clinical follow up under EU MDR
Adverse Events Reporting built into the platform
Leading-edge, open API for connecting study data to other clinical or quality systems
Greenlight Guru Clinical supports pre-market clinical investigations, post-market surveillance studies, registries, and human factors testing, and is used by both device and diagnostics manufacturers and by contract research organizations (CROs) that specialize in medtech. A validation package is included with every product update, removing the ongoing burden of software revalidation from the quality team. Every customer also gets a dedicated customer success manager with real medtech experience, not a generalist software account rep. For manufacturers already on Greenlight Guru's quality management system (QMS), Clinical extends into one connected platform spanning quality, product development, and clinical evidence.
Integrations Supported
BSI CTMS
ChatGPT
Claude
Claude Duet
Claude for Legal
Cursor
Gemini
Medidata
API Availability
API Availability
Has API
Pricing Information
$99/month
Various plans for different types of research projects.
Free Trial Offered?
Pricing Information
Pricing not provided
Free Trial Offered?
Supported Platforms
SaaS
Supported Platforms
SaaS
Customer Service / Support
Standard Support
Web-Based Support
Customer Service / Support
Standard Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Mosio, Inc.
Date Founded
2007
Company Location
United States
Company Website
www.mosio.com
Company Facts
Organization Name
Greenlight Guru
Date Founded
2013
Company Location
Denmark
Company Website
www.greenlight.guru/clinical-electronic-data-capture-software
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Enrollment Management
HIPAA Compliant
Monitoring
Scheduling
Contact Tracing
Forms / Surveys
Notifications
SMS / Email / Voice Communications
Wearable Integration
Electronic Data Capture
Not specified
Patient Engagement
Appointment Scheduling
Messaging
Progress Tracking
Remote Patient Monitoring
HIPAA Compliant
Patient Engagement
Patient Surveys
Reminders
Virtual Visits
Research Management
Not specified
SMS Marketing
2-Way Messaging
Contact Management
Mass Texting
Message Personalization
Shortcodes
Survey
Custom Survey URLs
Mobile Survey
Offline Response Collection
Question Branching
Skip Logic
Supports Audio / Images / Video
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Scheduling
Study Planning
Electronic Data Capture
Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management