Clinical Trial Software

Elevate the efficiency and accuracy of your clinical trials with Kohezion's Clinical Trial Management Software, a comprehensive solution designed to streamline trial processes and data management. For enhanced operational control and data-driven decision making.

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What is Clinical Trial Software

Kohezion's Clinical Trial Management Software is your all-encompassing solution for managing the complex processes of clinical trials. From patient recruitment and enrollment to data collection and analysis, this software simplifies each step. It facilitates seamless collaboration between researchers, sponsors, and regulatory bodies, ensuring compliance and efficiency. This Clinical Trial Software speeds of clinical research, making it an indispensable tool for any clinical trial operation.

Clinical Trial Software Features

Study Planning and Protocol Design

Assists in planning trial logistics, defining protocols, and ensuring adherence to study guidelines.

Participant Recruitment and Enrollment

Efficiently manage patient recruitment, track enrollment progress, and maintain participant data.

Regulatory Compliance Management

Ensure compliance with regulatory requirements, including documentation, approvals, and reporting.

Site Management and Monitoring

Facilitate site communication, monitor progress, and address any issues during the trial.

Data Collection and Management

Capture and organize trial data, including electronic data capture (EDC) and direct data capture (DDC).

Randomization and Blinding

Implement randomization protocols and maintain blinding to ensure unbiased results.

Clinical Supply Management

Track and manage drug supplies, equipment, and other resources needed for the trial.

Safety Monitoring and Adverse Event Reporting

Monitor patient safety, report adverse events, and ensure timely intervention.

How to use Clinical Trial Software

Trial Planning and Design

Participant Recruitment and Enrollment

Site Management and Monitoring

Data Collection and Electronic Data Capture (EDC)

Regulatory Compliance and Document Management

Budgeting and Financial Management

Study Analytics and Reporting

Collaboration Tools

Inventory and Supply Management

Clinical Trial Software is Designed For:

Clinical Trial Coordinators
Clinical Trial Managers
Clinical Project Managers
Clinical Trial Associates

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What is Next?

  • Get help building your app: Request a demo and we'll install this application to your trial Kohezion account. 
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iniversity of illinois

Frequently Asked Questions

Kohezion's Clinical Trial Management Software is your all-encompassing solution for managing the complex processes of clinical trials. From patient recruitment and enrollment to data collection and analysis, this software simplifies each step. It facilitates seamless collaboration between researchers, sponsors, and regulatory bodies, ensuring compliance and efficiency. This Clinical Trial Software speeds of clinical research, making it an indispensable tool for any clinical trial operation.

  1. Trial Planning and Design
    • Facilitate the planning and design of clinical trials, including protocol development, in the 'Trial Planning' module. Streamline trial setup processes to align with research objectives.
  2. Participant Recruitment and Enrollment
    • Manage participant recruitment, screening, and enrollment processes in the 'Participant Management' section. Efficiently track participant progress throughout the trial.
  3. Site Management and Monitoring
    • Oversee clinical trial sites and conduct monitoring activities in the 'Site Management' module. Ensure compliance with trial protocols and regulatory standards.
  4. Data Collection and Electronic Data Capture (EDC)
    • Collect clinical trial data using electronic data capture systems in the 'Data Collection' section. Ensure data accuracy and integrity.
  5. Regulatory Compliance and Document Management
    • Manage regulatory compliance and trial documentation, including the Trial Master File (TMF), in the 'Compliance' module. Streamline submissions to regulatory bodies.
  6. Budgeting and Financial Management
    • Control trial budgets, financial planning, and expense tracking in the 'Financial Management' section. Ensure efficient financial oversight of clinical trials.
  7. Study Analytics and Reporting
    • Analyze trial data and generate reports on study progress, enrollment, and outcomes in the 'Analytics' module. Utilize data for strategic decision-making.
  8. Collaboration Tools
    • Enhance team collaboration and communication among researchers, sponsors, and CROs using integrated tools in the 'Collaboration' section.
  9. Inventory and Supply Management
    • Manage trial supplies, including drugs and equipment, efficiently in the 'Inventory Management' module. Ensure adequate supply throughout the trial.
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