UK Explains Dos And Don’ts Of Remote Clinical Trial Monitoring

Much-Awaited Guideline Outlines Critical Functionalities For EHR Systems

Updated UK guidance describes the factors that clinical trial sponsors and investigator sites must consider when giving appointed representatives direct access to the electronic health records of participants in clinical trials to check source data.

Background image of computer screen showing electronic medical records application with computer lab
Digitization of medical records has enabled remote monitoring of trials • Source: Alamy

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