Siebel Life Sciences Guide > Regulatory Reporting >
Generating Regulatory Report Numbers and Submitting Reports (End User)
When you generate a 3500A or MDV initial report:
- The report number is generated and filled in
- The Status field changes to Submitted
- The fields in the regulatory report record become read-only (except for the Sub Status field)
Only the primary owner of the regulatory report can generate the report number and submit the report. This task is a step in Process of Regulatory Reporting. To generate and submit a regulatory report
- Make sure the application is running on a server database.
You cannot generate a report number on the Siebel Mobile Web Client.
- Navigate to Regulatory Reports screen > My Regulatory Reports view.
- Drill down on a regulatory report with status of In Progress.
- Click Generate.
This starts the LS Medical Product Issue RR Submit workflow, which authenticates the user, adds a number for the regulatory report, changes the status to Submitted, and makes all fields except Sub Status read-only.
For more information about the workflow, see LS Medical Product Issue RR Submit Workflow.
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