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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 OnCore?

Gain a thorough grasp of your research functions by implementing a comprehensive and standardized clinical trial management system that has been crafted in collaboration with leading academic medical and cancer institutions. Optimize billing designation workflows to facilitate consistency across different teams and platforms. Refine your budgeting methodologies, guarantee precise charge routing, and conduct more efficient audits and monitoring of billing compliance. This cohesive strategy offers extensive visibility and understanding of all facets of clinical research, especially in financial oversight, due to partnerships with top-tier research organizations. Additionally, by linking OnCore with your current electronic medical records (EMR), including smooth integrations with systems like Epic and Cerner, you can greatly enhance patient safety, reduce redundant data entry, improve billing compliance, and increase overall operational effectiveness. This advanced system not only streamlines processes but also cultivates a more productive research atmosphere, ultimately leading to improved outcomes in your clinical initiatives. Furthermore, the integration of these advanced technologies may lead to a more collaborative environment among research teams, fostering innovation and excellence.

Media

Media

Integrations Supported

ClinVigilant
IBM Datacap
XpertCoding

Integrations Supported

ClinVigilant
IBM Datacap
XpertCoding

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

Advarra

Date Founded

1993

Company Location

United States

Company Website

www.advarra.com/solutions-for/clinical-trial-sites/oncore-enterprise-research-ctms/

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

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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