The training aims to prepare the team for effective use of the eCRF system employed. The course introduces participants to the basic functionalities of the system and the standards for handling data in a clinical trial in an accessible manner.
The training covers, among others:
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Logging in and managing user accounts
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Overview of the eCRF system interface
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Entering, editing, and signing patient data
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Handling visit and adverse event forms
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Submitting and responding to queries
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Review of alerts and notifications
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Compliance with regulations (GCP, 21 CFR Part 11)
- Teacher: Admin Użytkownik