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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 LabRelations?

LabRelations stands out as a cutting-edge and versatile laboratory platform aimed at streamlining and enhancing scientific and testing processes through the integration of vital modules such as LIMS, ELN, CTMS, and EDC into a unified system that supports everything from sample tracking to experiment documentation, as well as study management and compliance reporting. This all-encompassing tool effectively reduces manual labor, minimizes inaccuracies, and eliminates data silos, allowing laboratories to centralize all pertinent information in one accessible location. Users can create workflow automations based on specific rules, connect instruments and external systems, and maintain comprehensive audit trails to ensure compliance with regulations like GxP and 21 CFR. Additionally, LabRelations offers the capability to customize objects, forms, views, and permissions according to the distinct needs of each laboratory, fostering improved collaboration across different functions while providing real-time insights that span research, quality assurance, clinical studies, and stringent regulatory environments. Consequently, this platform not only enhances operational efficiency but also bolsters the reliability of laboratory processes, paving the way for more innovative scientific advancements. By adopting LabRelations, laboratories can prepare themselves to meet future challenges with greater agility and effectiveness.

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

Merative

Date Founded

2022

Company Location

United States

Company Website

www.merative.com/clinical-development

Company Facts

Organization Name

LabRelations

Company Location

United States

Company Website

labrelations.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

Electronic Data Capture

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

ELN

LIMS

Audit Trail
Certificates of Analysis
Data Import / Export
Electronic Laboratory Notebook
Inventory Management
Lab Instrument Interface
Reporting & Statistics
Sample Tracking
Specification Management
Workflow Management

Medical Lab

Audit Trail
Data Analysis Auditing
Data Security
EMR Interface
Fax Management
Lab Instrument Interface
Multi-Location Printing
Online Instrumentation
Physician Test Panels
Procedure-Based Billing
Sample Tracking

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