Clinical Research Software

Our Clinical Research Software is designed to streamline research, study management and data analysis while being super flexible for your specific research needs. Experience efficiency and accuracy like never before in your research endeavors.

Use This Template
government case management software

What is Clinical Research Software

Kohezion's Clinical Research Software is an innovative solution for researchers and healthcare professionals. It offers an integrated platform for managing clinical research, from patient enrollment to data collection and analysis. The software provides robust tools for statistical analysis, ensuring high-quality, reliable results. With its advanced HIPAA-compliant data security measures, it is ideal for simplifying complex research processes, enhancing collaboration among researchers, and ensuring compliance with regulatory standards.

Clinical Research Software Features

Audit and Inspections

Tools for managing audits and inspections efficiently to ensure compliance with regulatory requirements.

Quality Assurance (QA) Support

maintaining data quality, adherence to protocols, and regulatory compliance through automated checks, validation rules, and data reconciliation.

Drag-and-Drop Study Designer

A user-friendly interface for designing study protocols, forms, and workflows.

Central and Local Laboratory Data Handling

Integrates laboratory data seamlessly, enabling efficient tracking and management of lab results across study sites.

Risk-Based Monitoring Tool

Helps prioritize monitoring efforts based on risk factors, optimizing resource allocation and ensuring data quality.

Collaboration and Communication Hub

A centralized platform for study teams, investigators, and sponsors to collaborate via document sharing and task management.

Real-Time Data Monitoring and Alerts

Monitor study progress, patient enrollment, adverse events, and data quality in real time.

Integrated Regulatory Compliance Tools

Compliant with regulations such as the Health Insurance Portability and Accountability Act (HIPAA).

How to use Clinical Research Software

  1. Study Design and Setup
    • Design and set up clinical research, trials, including protocols and methodologies, in the 'Study Design' module. Ensure alignment with research objectives and compliance standards.
  2. Participant Management
    • Manage participant recruitment, enrollment, and tracking in the 'Participant Management' section. Maintain participant data securely and manage consent forms.
  3. Data Collection and Management
    • Collect, store, and manage clinical trial data in the 'Data Management' module. Use electronic data capture (EDC) systems for efficient and accurate data collection.
  4. Regulatory Compliance and Submission
    • Ensure compliance with regulatory requirements and manage submissions to regulatory bodies in the 'Regulatory Compliance' section. Keep track of submission deadlines and requirements.
  5. Study Monitoring and Site Management
    • Oversee clinical study progress and manage site activities in the 'Study Monitoring' module. Conduct site visits and audits to ensure study integrity.
  6. Adverse Event and Safety Reporting
    • Track and report adverse events and safety incidents in the 'Safety Reporting' section. Ensure timely reporting in compliance with regulatory guidelines.
  7. Data Analysis and Statistical Reporting
    • Analyze clinical trial data and generate statistical reports in the 'Data Analysis' module. Utilize advanced statistical tools for comprehensive data interpretation.
  8. Document Management and eTMF
    • Manage study-related documents and maintain an electronic Trial Master File (eTMF) in the 'Document Management' section. Ensure easy access and organization of critical documents.
  9. Financial Management and Budgeting
    • Handle financial aspects of clinical trials, including budgeting and invoicing, in the 'Financial Management' module. Track study costs and manage funding.
  10. Collaboration and Communication Tools
    • Facilitate collaboration among research teams, sponsors, and stakeholders using integrated communication tools in the 'Collaboration' section.

Clinical Research Software is Designed For:

Clinical Research Coordinators
Clinical Research Managers
Research Nurses
Clinical Research Associates

Related Healthcare Software

What is Next?

  • Get help building your app: Request a demo and we'll install this application to your trial Kohezion account. 
Use This Template
clark
yale
harvard
marine mammal
university of san francisco
iniversity of illinois

Frequently Asked Questions

Kohezion's Clinical Research Software is an innovative solution for researchers and healthcare professionals. It offers an integrated platform for managing clinical research, from patient enrollment to data collection and analysis. The software provides robust tools for statistical analysis, ensuring high-quality, reliable results. With its advanced HIPAA-compliant data security measures, it is ideal for simplifying complex research processes, enhancing collaboration among researchers, and ensuring compliance with regulatory standards.

  1. Study Design and Setup
    • Design and set up clinical research, trials, including protocols and methodologies, in the 'Study Design' module. Ensure alignment with research objectives and compliance standards.
  2. Participant Management
    • Manage participant recruitment, enrollment, and tracking in the 'Participant Management' section. Maintain participant data securely and manage consent forms.
  3. Data Collection and Management
    • Collect, store, and manage clinical trial data in the 'Data Management' module. Use electronic data capture (EDC) systems for efficient and accurate data collection.
  4. Regulatory Compliance and Submission
    • Ensure compliance with regulatory requirements and manage submissions to regulatory bodies in the 'Regulatory Compliance' section. Keep track of submission deadlines and requirements.
  5. Study Monitoring and Site Management
    • Oversee clinical study progress and manage site activities in the 'Study Monitoring' module. Conduct site visits and audits to ensure study integrity.
  6. Adverse Event and Safety Reporting
    • Track and report adverse events and safety incidents in the 'Safety Reporting' section. Ensure timely reporting in compliance with regulatory guidelines.
  7. Data Analysis and Statistical Reporting
    • Analyze clinical trial data and generate statistical reports in the 'Data Analysis' module. Utilize advanced statistical tools for comprehensive data interpretation.
  8. Document Management and eTMF
    • Manage study-related documents and maintain an electronic Trial Master File (eTMF) in the 'Document Management' section. Ensure easy access and organization of critical documents.
  9. Financial Management and Budgeting
    • Handle financial aspects of clinical trials, including budgeting and invoicing, in the 'Financial Management' module. Track study costs and manage funding.
  10. Collaboration and Communication Tools
    • Facilitate collaboration among research teams, sponsors, and stakeholders using integrated communication tools in the 'Collaboration' section.
Scroll to Top