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What is eAdjudication?

Ethical eAdjudication is a state-of-the-art software solution designed for endpoint adjudication and the requirements of e-clinical applications. Tailored for study leaders, quality assurance teams, and committee members, this cloud-based platform offers an incredibly intuitive interface. It aids in the efficient management of event databases, supports committee evaluations, and organizes discussions aimed at resolving conflicts and reaching consensus within a GxP compliant environment. By leveraging Ethical eAdjudication, users can conduct independent reviews and adjudication processes with ease, ensuring prompt outcomes while upholding stringent quality control measures. This groundbreaking platform not only optimizes workflows but also fosters enhanced collaboration and decision-making among all involved parties. Ultimately, it represents a significant advancement in the realm of clinical research technology.

What is ClinVigilant?

Enhance the efficiency of your clinical studies with Clinvigilant, your global provider of budget-friendly eClinical tools tailored for CROs, Pharma, Biotech, Nutraceuticals, and academic institutions throughout both clinical and post-marketing phases. Our clients consistently choose to partner with us due to our: ♦ Rapid EDC implementation (under 4 weeks). ♦ Cost-effective solutions. ♦ Integration capabilities with third-party and legacy systems. Our cloud-based platform, hosted on Microsoft Azure, adheres to HIPAA, ICH-GCP, GDPR, and 21 CFR part 11 regulations and has successfully undergone audits by the FDA, EMA, and MHRA. The Clinvigilant eClinical suite encompasses a variety of tools, including EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent, and eCOA. You can select the specific tools you require, and we will seamlessly integrate them into your existing software framework. Each interaction and data exchange generates detailed Audit Trails, ensuring real-time visibility of compliant data across all relevant roles. Our offerings are modular, highly customizable, and accessible via web, iPad, and mobile applications for both Android and iOS platforms. Additionally, we support the use of Patient's Own Devices (BYOD) and can interface with various devices and wearables for enhanced data collection. With Clinvigilant, you can count on a comprehensive solutions provider to streamline your clinical trial processes effectively and efficiently. Your success in clinical research begins here.

Media

Media

Integrations Supported

Medidata
Medrio
OpenClinica
Oracle API Catalog
REDCap
Veeva Vault
Zelta

Integrations Supported

Medidata
Medrio
OpenClinica
Oracle API Catalog
REDCap
Veeva Vault
Zelta

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
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

Ethical

Date Founded

2013

Company Location

Switzerland

Company Website

www.ethical.ch

Company Facts

Organization Name

ClinVigilant

Date Founded

2017

Company Location

United Kingdom

Company Website

www.clinvigilant.com

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

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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