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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A Master 100% HIPAA-Compliant System for Your Clinical Trial Operational Needs.

Streamline workflows, administrative tasks, and clinical trial management with our all-in-one solution.

Highlights of Clinical Trials Software

Designed to transform clinical trial management, Kohezion's Clinical Trial Software focuses not only on operational efficiency but also on advancing the quality of research outcomes. It provides researchers with real-time data insights, enabling quicker adjustments and more informed decisions. The software's adaptability to various trial designs and scalability makes it suitable for a range of clinical studies, from early-phase trials to large-scale international studies and medical device companies.

Clinical Trial Management
Data Management
Regulatory Compliance
Patient Recruitment

Electronic data capture software for clinical trials

Our nodule for Electronic Data Capture Software revolutionizes data management in clinical trials. It's engineered to facilitate rapid, accurate data collection, reducing manual errors and increasing efficiency. The platform supports real-time data entry and validation, ensuring high data quality and integrity. Ideal for diverse clinical trial phases, it offers customizable forms and reports, making it adaptable to various research requirements.

Clinical data management software

There's another feature that is of interest, and that is our Clinical Data Management software module. It's a comprehensive solution for handling complex data challenges in clinical research. It facilitates efficient data collection, validation, and analysis, ensuring the integrity and reliability of research data. With features like customizable data entry forms, robust data cleaning tools, the software is essential for managing the vast amounts of data generated in clinical trials.

Clinical Trial Software Modules

Clinical Trial Software

Key Features of Clinical Trial Software

  1. Optimizes patient recruitment and enrollment processes for diverse clinical trials.
  2. Manages vast amounts of trial data efficiently, ensuring accuracy and accessibility.
  3. Assures compliance with all regulatory and ethical standards in clinical research.
  4. Provides real-time data analytics for timely and informed decision-making.
  5. Facilitates collaboration and communication among all stakeholders in a trial.
  6. Scales to accommodate various trial sizes and complexities, adapting to evolving research 

Clinical Trial Management Software Capabilities

Trial Management Dashboard
Automated Regulatory Reporting
Integrated Participant Tracking
Customizable Workflow Management
Secure Data Storage and Transfer
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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. 

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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