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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.

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

Google Sheets
Medidata
Microsoft Excel
OpenClinica
TrialMaster
Veeva CRM

Integrations Supported

Google Sheets
Medidata
Microsoft Excel
OpenClinica
TrialMaster
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

Anju Software

Date Founded

2016

Company Location

United States

Company Website

www.anjusoftware.com/ctms

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

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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