Managing clinical trials involves the tracking of a large database of secure information. Key Solutions’ Clinical Trials software offers a centralized site for accurately and efficiently managing and tracking all your clinical trials data; accelerating research, improving reports, and maintaining ethical and regulatory compliance.

Team members have access to a common portal through which they can view study design, data collection, and patient contact information, medical records and consent forms. The module automates all of the billing, invoicing and budget tracking for participant payment, sponsor payments and integration to clinical billing systems.

Our Clinical Trials Management System is fully-integrated with our Research Compliance Software for Human Subjects (IRB) assuring that your research meets all ethical and regulatory standards.

Key Highlights:

• Online development of study design and parameters
• Online budget creation, routing and approval
• Electronic subject enrollment and status and patient contact information
• Clinical data collection via PC, PDA or Tablet PC
• Integration with Case Report Form (CRF)
• Automated invoicing and payment of patients, sponsors and third-party billing systems
• Automated tracking and reporting