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What is ArcheMedX Ready?

ArcheMedX offers a solution designed for pharmaceutical and biotech trusts to enhance the effectiveness of their trial teams, streamline decision-making processes, and minimize delays in studies. By identifying the most capable sites and teams for conducting trials, organizations can sidestep common pitfalls that lead to study postponements. This approach not only cuts down on the time and expenses associated with problem resolution, particularly in the early phases of a trial, but also ensures that selected sites have a thorough understanding of patient eligibility criteria. Consequently, you can trust that they are better positioned to enroll suitable patients more efficiently, achieve enrollment goals, and reduce screen failure rates. Additionally, the trial team’s deep familiarity with the study protocol and its specific objectives fosters a comprehensive understanding of the project. This proactive strategy allows for the anticipation of potential risks, enabling teams to mitigate them effectively and ultimately resulting in fewer deviations throughout the trial process. Overall, this systematic preparation leads to a smoother and more successful trial execution.

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

ArcheMedX

Date Founded

2013

Company Location

United States

Company Website

www.archemedx.com

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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