Our ClinPlus CTMS was developed to improve user accessibility and communications on clinical trial operations data. By adding ClinPlus CTMS to your clinical trial toolbox, tremendous efficiencies and time savings can be realized, manual operations can be reduced, and redundant data and tasks will be eliminated.

• Provides cost-effective, compliant Web access to global trials
• Expedites trial design and study set-up
• Efficiently collects and manages patient and trial data
• Truly Integrated Site Visit Report tools
• Tracks documents and alerts you about missing and expiring documents  
• Manages budgets, payments, vendor costs, pass-thru costs, etc. 
• Track study inventory
• Study and Site "blogs" add structure to your communications logs
• Advanced standard and custom reporting including automated, scheduled delivery.
• Supports custom fields for complete adaptability