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What is Rave EDC?

Medidata's Rave EDC (Electronic Data Capture) is recognized as the leading system for effectively handling clinical trial data from various sources like sites, patients, and laboratories, ensuring both sophistication and security. As a key component of the Medidata Clinical Cloud™, it provides an all-encompassing platform that harmonizes multiple processes, thus removing the need for data reconciliation and enabling thorough data analysis across various studies and functions. Users are able to manage their responsibilities, studies, and sites through a unified dashboard that integrates all Rave EDC and other Medidata Clinical Cloud tools. This platform significantly reduces the risks of duplicate study master data and discrepancies, such as inconsistent IDs for identical sites across different applications. Central to Medidata’s unified strategy for Clinical Data Capture and Management, Rave EDC supports the smooth collection and reconciliation of data from an array of sources, including Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; it also bolsters data review and analysis with sophisticated tools like Rave TSDV and Medidata Detect. By offering these advanced functionalities, Rave EDC not only streamlines the data management process but also empowers clinical researchers to make well-informed decisions grounded in trustworthy and comprehensive data insights. Therefore, it plays an essential role in enhancing the overall efficiency and effectiveness of clinical trials.

What is Jeeva eClinical Cloud?

Jeeva has developed a revolutionary modular system that operates on a cutting-edge cloud platform. With just one login from any device that supports a browser, users can easily screen patients, offer education, manage enrollment, send SMS and emails, and compile evidence such as electronic patient-reported outcomes. Frustrations with slow patient recruitment and retention are common in the industry, making it imperative to gather solid evidence of safety and efficacy for new investigational medicines to secure approval from regulatory agencies. Jeeva stands out as an invaluable resource for optimizing time and financial resources for patients and biopharma sponsors, particularly in long-term follow-up studies associated with gene therapy. Its innovative approach streamlines processes, ultimately enhancing the efficiency of clinical trials and improving patient care.

Media

Media

Integrations Supported

AWS Auto Scaling
AWS Backup
Django
GitHub
Google
Google Maps
Medidata
Python
Rave CTMS
React Native
SendGrid
Twilio
Twilio Messaging
Twilio Voice
nOps

Integrations Supported

AWS Auto Scaling
AWS Backup
Django
GitHub
Google
Google Maps
Medidata
Python
Rave CTMS
React Native
SendGrid
Twilio
Twilio Messaging
Twilio Voice
nOps

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$100/mo/user
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Dassault Systèmes

Date Founded

1981

Company Location

France

Company Website

www.medidata.com/en/clinical-trial-products/clinical-data-management/edc-systems

Company Facts

Organization Name

Jeeva Informatics Solutions

Date Founded

2019

Company Location

United States

Company Website

jeevatrials.com/solutions/

Categories and Features

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
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

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