Streamlining electronic reporting of serious adverse events (SAEs) using the REDCap data collection system: the eSAE Project
<p><strong>Background: </strong>It is essential that electronic data collection (EDC) systems are both compliant with regulations and the principles of Good Clinical Practice (GCP) to allow for the timely and accurate reporting of data including safety data. For clinical trials of...
| Main Authors: | , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
BioMed Central
2024
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