Improve Critical Study Objectives

• Patient Compliance
• Patient Engagement
• Safety Management
• Data Management

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eSource In Clinical Trials | Support FDA Guidance

According to the FDA guidance on source data in electronic form, eSource will help to eliminate unnecessary duplication of data, reduce the opportunity for transcription errors, promote the real-time entry of electronic source data during subject visits, ensure the accuracy and completeness of data, and more.

assisTek's TotalSource solutions capture these improvements to source data, and are customized to each individual protocol.

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