Edit a Site

Entering Data ›› Data Entry ››
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If sites have been previously entered, you’ll see the sites landing page like the one in Figure 1 below.


Figure 1: All Sites Landing Page

In this screen (Sites tab) a number of columns are visible with data that summarizes each investigative site.  See the table below.

Name

The name of the site.

Num

The site number, if one has been assigned.

Status

The current status of the site (Candidate, Qualified, Waiting IRB, Active, Suspended, Closed).

Subjs

The number of active subjects at the site.

Activation

Date of site’s activation.

First Enroll

Date of first subject’s enrollment.

Last Enroll

Date of last subject’s enrollment.

Version

The version of the database currently used at a site.  



To edit a site, click on the underlined name of the site which contains a hyperlink that will navigate you to form for that site.  To edit the site, click on Edit Site under Actions in the side bar.  See Figure 2 below.


Figure 2: Actions: Edit Site


There are additional fields in the Edit Site screen that are available when the site is created.  See Figure 3 below.


Figure 3: Edit Site Screen


Additional fields/sections below are available in the Edit Site mode that are not available in the Create Site mode.

First Enroll Date

The date the first subject was enrolled.

Enrollment Stop Date

The date enrollment was discontinued at the site.

Close Out Date

The date the site was considered closed.

Online Message


This message will appear at the top of the site landing page.  It remains active until removed from this field.

Email Group Section

Email addresses of individuals assigned to groups for email notifications.  An unlimited number of email may be entered, separated by a comma.  (Email groups may be set up for the purpose of notifying the parties of pertinent study events, such as the enrollment of a subject, reporting of an adverse event or protocol deviation.  There are three potential email groups available that could be assigned to an event.)

Sponsor Resource

Main sponsor contact for the clinical trial.