Clinical monitoring, powered by our people and platform.
Loopa delivers clinical monitoring through our own monitors and proprietary platform. The platform checks the source data you provide against study requirements and across sources. Our monitors assess potential issues, document decisions, and follow up with sites.
Discuss monitoring for your study
Source review starts with the study’s requirements.
Loopa-led monitoring. Or our platform for your team.
Clinical monitoring, delivered by Loopa.
Our monitors work on our proprietary platform, with monitoring scope agreed for your study. For sponsor teams with established monitoring operations, platform licensing is also available.
For sponsors
Technology for your monitoring teams.
License Loopa’s platform to support requirements-driven source review. Your monitors assess potential issues and make the decisions.
For CROs
See the platform behind the model.
Explore the workflow from source evidence to monitor review.
From study requirements to documented decisions.
The platform prepares the evidence. Monitors apply their judgment.
Organize study requirements for review, with traceability to the source document. A monitor reviews and accepts the requirements baseline.
Check the source data provided against those requirements and across documents. Potential issues become Loops with supporting evidence.
A monitor assesses each Loop in context, records the decision and reasoning, and determines the appropriate follow-up.
Record review decisions and follow-up in the study workflow.
EDC Verification compares source information with EDC data through an available read-only connection.
See the full walkthrough
Illustrative requirements mapped from a synthetic protocol.
Illustrative source document with a potential issue highlighted.
Illustrative Loop presented for monitor assessment.
Illustrative Finding workflow using synthetic data.
“I’ve seen weeks of source sit unread between monitoring visits.
A visit would happen, and nine or ten weeks would go by before the monitor came. That is when the queries were raised, on work we had done two months earlier. Then came the pressure to close every one of them fast. The sponsor was the last to know anything was wrong.
So we built Loopa to read every document within minutes of receipt, not a sample of them. It is the only version of this I would have trusted when I was the one sitting across from the inspector.”
Source review between monitoring visits.
The platform prepares source evidence for review, helping monitors focus their assessment before and between visits.
Quality first. Velocity and value follow.
Evidence connected to judgment.
Study requirements, source evidence, and monitor decisions brought together for review.
- Mapped requirements
- Supporting evidence
- Documented decisions
Prepared for review.
The platform assembles evidence and potential issues so monitors can focus their assessment before and between visits.
Focus clinical expertise.
Define the monitoring scope and evaluate the business case for your study.
The latest from Loopa.
Discuss monitoring for your study.
Talk with us about Loopa-led monitoring or licensing the platform for your own team.