You want to identify
- Risks to your clinical trial data in order to mitigate them before they become issues
- Issues that affect data integrity
Our work with electronic records and systems gives us the experience you need to identify risks and issues.
Linking risks and issues to GCP requirements helps you report effectively to audiences with various levels of understanding and areas of responsibility.
Our experience in statistics, programming, validation, SOP writing, and auditing helps you make those linkages.
A picture is worth a thousand words. We can visually interpret processes and issues using flow diagrams built into the audit report or in presentation format.
This further facilitates communication with your executive team so you can focus on remediation and safeguarding your clinical trial.