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About Allegro CTMS

Allegro CTMS is a clinical trial management software from Forte Research Systems that supports the management of clinical trials. It combines study management, data collection, and regulatory compliance functionalities so users can efficiently oversee clinical research processes. The platform provides tools for tracking study progress, managing site communications, and handling document submissions. Allegro CTMS is designed to facilitate collaboration among research teams and ensures compliance with industry regulations. It offers customizable reporting features that allow for real-time insights into study performance. Key capabilities: study management document tracking site communication regulatory compliance reporting tools Best for: clinical research organizations that need a comprehensive solution for managing clinical trials.

Allegro CTMS Details

Vendor
Forte Research Systems
Year Launched
Location
539 Science Drive, Suite 200, Madison, WI 53711
Deployment
Training Options
demo, account manager, community
Countries Served
All Countries
Languages
English, Spanish, French, German, Italian, Portuguese, Japanese
Users
Clinical Researchers, Study Coordinators, Principal Investigators, Data Managers, Research Nurses, Regulatory Compliance Staff, Clinical Trial Monitors.
Industries Served
Healthcare, Research, Life Sciences
Tags
Clinical Trial Management, Allegro CTMS, Forte Research Systems

Allegro CTMS's In-App Market Place

Does Allegro CTMS have an in-app market place?

Yes

How many Mini-Apps in the marketplace?

5

Mini Apps

1. Budgeting Module: A tool that helps streamline budget creation and management for clinical trials within Allegro CTMS.

2. eReg Binder: An electronic regulatory binder add-on that organizes and tracks essential documents required for compliance.

3. Monitoring Visit Report Generator: Generates automated monitoring visit reports to track site visits and ensure protocol compliance.

4. Query Management System: A tool for managing and resolving queries related to data collection and entry in clinical trials.

5. Risk-Based Monitoring Module: A module that allows for implementing risk-based monitoring strategies to improve trial efficiency and data quality.

Pricing Options

Free trial
Free version
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Accepted Payment Currencies

USD ($), EUR (€), GBP (£), AUD (A$), CAD (C$), JPY (¥), CNY (¥), SGD (S$), HKD (HK$), CHF (Fr), SEK (kr), DKK (kr), NOK (kr), KRW (₩), INR (₹), NZD (NZ$), MXN (Mex$), BRL (R$)

Pros & Cons

  • Streamlines clinical trial operations and management
  • Improves efficiency and accuracy of data collection and analysis
  • Enhances collaboration among research team members
  • Provides real-time visibility into study progress and performance
  • Helps ensure compliance with regulatory requirements and protocols
  • Facilitates communication with study participants
  • Enables better decision-making based on comprehensive study data
  • Increases overall study success rates by optimizing processes and workflows
  • Limited customization options for study workflows
  • Steep learning curve for new users
  • Lack of integration with other clinical trial management tools
  • Limited reporting capabilities
  • Technical support can be slow to respond to user inquiries

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