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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 Clinipace?

At Clinipace, we offer a distinctive level of teamwork and oversight that significantly surpasses the standards found in traditional contract research organizations. Our goal is to adeptly navigate you through the intricate processes of your clinical development initiatives. As a comprehensive global CRO, we emphasize a tailored approach to clinical research. We focus on adaptability and cooperation, bolstered by our extensive regulatory knowledge and expertise across a variety of therapeutic fields. Our aim is to revolutionize the clinical research landscape in areas such as oncology, rare diseases, gastroenterology, nephrology, and women's health. By harnessing state-of-the-art technology and a flexible approach, Clinipace is committed to influencing the future of drug development and improving health care results. Our dedication to pioneering solutions allows us to stay ahead in industry advancements, ultimately benefiting the patients we serve. In this rapidly evolving environment, we strive to maintain our leadership position while fostering innovation at every step.

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

Clinipace

Date Founded

2003

Company Location

United States

Company Website

www.clinipace.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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