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Event Details


The Role of Data, Content, and Workflow in Selecting Study Sites

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Who should attend?

Senior professionals working with clinical data/clinical documentation, including: Trial Master File (TMF) Management Clinical Records Management Clinical Trial Management Clinical Operations Clinical Trials Associates (CTA’s) / Clinical Research Associates (CRA’s) Site Management Study / Study Start-up (SSU) Management


Join Veeva’s Ashley Davidson and Paragon’s Chris McSpiritt to hear how adopting the right technology can help you avoid these delays. Discussions will include how to use content, data, and workflow together to significantly optimize the selection and activation processes.




Andrew Juurinen

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