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What is eDeviation?

eDeviation offers a thorough suite of tools designed for the evaluation and management of Protocol Deviations, simplifying the journey from software development and validation to the collection of essential documentation and the exportation of data for the Trial Master File (TMF). This innovation significantly reduces the workload on clinical teams who may encounter risks associated with poorly evaluated or neglected protocol deviations, regardless of their frequency. As part of Ethical's eClinical Software Platforms, eDeviation® improves the precision and productivity of clinical trial oversight. The software can be customized to fit the unique needs of your research team, whether assessments are made by an independent committee or internally. Its built-in forms, workflows, and export capabilities guarantee compliance with GxP standards while promoting effective study management. Moreover, the platform supports real-time online collaboration among study teams, investigators’ sites, and committee members, which accelerates decision-making and ensures that protocol deviation assessments are addressed promptly. This collaborative environment not only streamlines processes but also fosters a culture of transparency and accountability in clinical trials. Ultimately, eDeviation® plays a crucial role in enhancing the integrity and efficiency of clinical research processes, leading to improved research outcomes.

What is Zelta?

Zelta serves as a cloud-based platform dedicated to the unified management and acquisition of clinical data, aiming to optimize and improve the processes involved in clinical trials. Its flexible modular structure is tailored to meet the specific requirements of different studies, which leads to quicker and more effective results. With features that include electronic data capture, management of clinical operations—such as randomization and tracking of trial supplies—clinical trial oversight, and electronic trial master file capabilities, Zelta provides thorough supervision of studies. Additionally, it fosters engagement among patients and providers through electronic clinical outcome assessments and e-consent options. Suitable for a range of studies across all phases, therapeutic disciplines, and international locations, Zelta is designed to offer a user-friendly experience with secure single sign-on access available from any location. Its adaptable and scalable framework permits easy customization and seamless integration with both proprietary and third-party technologies, ensuring it can meet various research requirements effectively. This makes Zelta an invaluable tool for researchers looking to streamline their clinical trial efforts.

Media

Media

Integrations Supported

ClinVigilant
IBM Datacap

Integrations Supported

ClinVigilant
IBM Datacap

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

eDeviation

Company Website

www.protocoldeviation.com/eDeviation-software

Company Facts

Organization Name

Merative

Date Founded

2022

Company Location

United States

Company Website

www.merative.com/clinical-development

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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