Raptim Research
Clinical Trial Management System (CTMS)
CTMS is a suite of eClinical tools that, are most effective on following part:
• Project Plan & Track
• Monitoring Planning & Management
• Contract & Milestone Tracking (Sites & Teams)
• Subject Visit Tracking
• Document Management
Raptim Research
Electronic Trial Master File (eTMF)
An eTMF is a Trial Master File in electronic format. It is a way of electronic capturing, managing, sharing and storing essential documents and content related to clinical trials. Global, real-time access, the ability to manage study files and document workflows, collaborate, and maintain all essential metadata and audit trails are a few reasons why using an electronic format is preferred by regulatory agencies and also by organisations.
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Raptim Research
Remote Source Data Verification (rSDV)
With the challenges of Covid-19 pandemic, regulatory authorities are suggesting remote approaches to conducting studies and more and more trials are looking forward to utilising remote technologies. By conducting SDV remotely, we go one more step ahead with a riskbased approach in clinical trials. With RBM techniques it helps to improve the data integrity. With this tool, it is possible for multiple site’s source data to be checked at a single centralization location without physically visiting a particular site.
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CRED-Bio Raptim Research
Advantages:
• Complete tracking of the volunteer database and records
• Convenient sample management as data samples come in a neat format
• One central place to review study-related data
• No manual intervention needed, minimizes the chance of error
• Easier movement tracking
• All acceptance is handled by the system
• Eliminates the chances of backup skip or deviation
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