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What is ClinAccess?

ClinAccess™ 5.1 marks a significant advancement in our leading Clinical Data Management System, which is entirely constructed on the powerful SAS® 9 framework. This cutting-edge system enhances the efficiency of clinical data management, streamlines the analysis of clinical trials, and simplifies the preparation of electronic submissions. By allowing data entry to be performed directly into SAS® data sets, it eliminates the tedious task of transferring data from Oracle/SQL to SAS, greatly increasing your team's productivity. ClinAccess™ is designed with user-friendly features for study definitions, data entry, and management, including tools that monitor the progress and quality of ongoing clinical trials. Your data remains consistently organized within SAS® for straightforward access, whether it’s for review, analysis, or submission to regulatory bodies like the FDA. The database architecture is finely tuned to enable swift statistical analysis and reporting, ensuring users experience a significant reduction in the time and effort needed for data analysis, which can accelerate the overall time to market. Furthermore, ClinAccess™ is distinguished by its reliability, extensive auditing functionalities, and strong security protocols, making it an exceptional option for managing clinical data. With ClinAccess™, you can adeptly handle the intricacies of clinical trials while upholding data integrity and compliance standards, thereby ensuring the success of your research endeavors. This comprehensive system empowers organizations to achieve milestones with confidence in their data management processes.

What is CTMS Master?

CTMS Master stands out as the leading clinical trial management system, crafted to tackle the intricate technical issues associated with managing clinical trials. By enhancing user communication, minimizing manual tasks, and eradicating redundant data, CTMS Master streamlines the overall trial process. This system not only improves efficiency but also features a Site Visit Report tool that works seamlessly with an automated workflow to avoid any duplicate data entry. Additionally, it simplifies the generation and distribution of ready-to-use Site Visit Reports (SVR). Users can utilize standard templates for various documents related to sites and projects, including budgets, events, milestones, and reports on site visits. With CTMS Master, you gain access to over 100 metrics and statistics designed to monitor clinical study sites, countries, and projects effectively. Furthermore, it comes equipped with more than 80 standard reports and offers ad-hoc reporting options for customized insights. Users can also develop site-specific budgets based on a default template, track both accrued and future obligations, and establish either automatic or manual approval processes for each payment type, ensuring thorough financial oversight throughout the trial. This comprehensive approach not only enhances transparency but also fosters better decision-making in clinical trial management.

Media

Media

Integrations Supported

TrialMaster

Integrations Supported

TrialMaster

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

MAJARO InfoSystems

Date Founded

1987

Company Location

United States

Company Website

www.majaro.com/html/clinical-data-management-software/clinaccess.html

Company Facts

Organization Name

Anju Software

Date Founded

2016

Company Location

United States

Company Website

www.anjusoftware.com/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

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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