Siebel Life Sciences Portals Guide > Site Portal > Adding Clinical Trial Subjects and Managing Subject Visits and Activities >

Enrolling Subjects

A subject who has successfully passed screening or rescreening is then enrolled in the study.

NOTE:  Enrollment activities cannot be generated without an informed consent date for the active version of the protocol.

To enroll a subject

  1. In the Subjects list on the eTrials page, select the subject.
  2. Click Apply Active Version.

    3. This creates new records in the informed consent field for all subjects in this site except those whose status is Early Terminated or Completed.

  3. Click the icon in the Informed Consent Dates field of the subject's record.

    4. The Informed Consent dialog box appears.

  4. Click New.

    5. The Add Informed Consent dialog box appears, showing the active version at the site.

  5. Click Add.

    6. The active version at the site appears in the Informed Consent dialog box.

  6. Enter an informed consent date, and then click OK.
  7. Click Enroll.

    8. The Enrollment dialog box appears.

  8. Enter the enrollment date and enrollment ID, and then click OK.
  9. Modify subject visit dates and activities if desired.

 Siebel Life Sciences Portals Guide 
 Published: 18 April 2003