{"id":481861,"date":"2024-01-10T13:43:05","date_gmt":"2024-01-10T18:43:05","guid":{"rendered":"https:\/\/platohealth.ai\/implementing-esource-a-guide-for-operations-and-technology-roles\/"},"modified":"2024-01-10T19:08:08","modified_gmt":"2024-01-11T00:08:08","slug":"implementing-esource-a-guide-for-operations-and-technology-roles","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/implementing-esource-a-guide-for-operations-and-technology-roles\/","title":{"rendered":"Implementing eSource: A Guide for Operations and Technology Roles","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"
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There\u2019s no doubt eSource has the potential to streamline the process of clinical research by improving efficient and accurate data collection. Eliminating the requirement for manual data transcription leads to significant savings in terms of the costs and time spent on a study.<\/p>\n

However, adopting eSource is challenging for many research facilities. Successfully implementing eSource requires sites to shift from paper-based data to electronic data records in a way to preserve data integrity and patient safety.<\/p>\n

Best Practices for Implementing eSource<\/h2>\n

eSource must be implemented in a way to ensure data reliability and trustworthiness. To achieve this, sites should adhere to the eSource principles of use<\/a>.<\/p>\n

Use \u201cFit for Purpose\u201d Solutions<\/h3>\n

The chosen method of eSource documentation should align with a trial\u2019s specific needs. Factors to consider include:<\/p>\n