Get the free REDCap: CT.gov Adverse Event Reporting Module

Supplemental Figure 1 Redcap Questionnaire COG Adverse Event Reporting Survey Please select your COG institution: TIP: Typing the first 2 or 3 letters of your institution\'s name will navigate through

How to fill out redcap ctgov adverse event

How to fill out redcap ctgov adverse event

1. Log in to RedCap CTGov using your credentials.
2. Navigate to the Adverse Events tab in the study project.
3. Click on the 'Add New Event' button to start filling out a new adverse event form.
4. Enter the details of the adverse event including event date, severity, outcome, and any relevant notes.
5. Save the adverse event form once all the required information has been entered.

Who needs redcap ctgov adverse event?

1. Researchers conducting clinical trials or studies that collect adverse event data need to use RedCap CTGov adverse event module.

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What is redcap ctgov adverse event?

Redcap ctgov adverse event refers to the reporting of any unexpected or unfavorable medical occurrence in participants of clinical trials.

Who is required to file redcap ctgov adverse event?

Researchers, sponsors, and healthcare providers involved in clinical trials are required to file redcap ctgov adverse event reports.

How to fill out redcap ctgov adverse event?

Redcap ctgov adverse event forms should be completed with detailed information about the adverse event, including the date of occurrence, severity, and any treatment provided.

What is the purpose of redcap ctgov adverse event?

The purpose of redcap ctgov adverse event reporting is to ensure the safety of participants in clinical trials and to monitor and manage any potential risks.

What information must be reported on redcap ctgov adverse event?

Information such as the nature of the adverse event, any medications or procedures involved, and the impact on the participant's health should be reported on redcap ctgov adverse event forms.