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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.

What is BioGRID?

BioGRID stands out as a sophisticated platform for managing clinical data and visual analytics, designed to streamline the management of clinical information and improve decision-making. By merging state-of-the-art AI technology with intuitive visual tools, stringent compliance functionalities, and optimized workflows for clinical trials, it fosters a seamless operational environment. This solution aggregates diverse clinical data sources, ensuring continuous data flow, trend analysis, forecasting, and predictive insights that enable teams to detect patterns and potential risks, thereby promoting proactive decision-making. Furthermore, BioGRID provides in-depth oversight of research studies, offering a detailed perspective on progress and outcomes, complemented by automated systems for patient tracking and resources for effective medical and statistical analysis. It also emphasizes active data monitoring and quality management based on risk, which plays a crucial role in preserving data integrity and adhering to industry standards by tracking key risk indicators, spotting potential inconsistencies, and ensuring thorough audit trails. By empowering clinical teams with the tools they need, BioGRID facilitates a confident and precise navigation through the complexities of data landscapes. In essence, BioGRID not only simplifies data management but also enhances the overall efficiency of clinical trials and research initiatives.

Media

Media

Integrations Supported

ClinVigilant
Google Sheets
IBM Datacap
Medidata
Microsoft Excel
OpenClinica
Veeva CRM

Integrations Supported

ClinVigilant
Google Sheets
IBM Datacap
Medidata
Microsoft Excel
OpenClinica
Veeva CRM

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

Merative

Date Founded

2022

Company Location

United States

Company Website

www.merative.com/clinical-development

Company Facts

Organization Name

BioGRID

Date Founded

1998

Company Location

Israel

Company Website

biogridsolutions.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

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

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