50.34 version 2.0 | FEMB Specimen Submission Form Training Guide
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Overview
Training Objectives
Upon completion of this material, users will be able to:
List the overall improvements CDC ID laboratories are making to the specimen accessioning and reporting process
Enumerate the benefits of using the new electronic Adobe specimen submission form
Enter the necessary information on the updated submission form
Link to the CDC Test Directory for essential information when ordering a test
Changes to the overall process
Changes to the overall process include:
The 3
rd
barcode encodes page 2 of the Specimen Submission form, not the Intermediate Submitter information. Therefore the
Intermediate Submitter information will be manually uploaded by CDC recipients.
Submitter information is a dropdown menu selection.
The “State PHL…”, “Original Submitter”, and “Intermediate Submitter” sections now contain a direct phone number and email address
for the Point of Contact, and no longer contain a phone number for the institution.
Updated Test Directory of Services
Enhancements that were implemented for Form 50.34 Version 2.0:
Federal, State, and International Submitters can now use the dropdown feature for Institution Name, allowing users to select their
Institution. Institutions are listed in alphabetically and users can easily find their Institution by typing the first letter of their state.
Selecting Institution Name from the drop-down menu causes the Address, Fax, and Institutional Email fields to be auto-populated with
contact information from standardized submitter records.
The ‘Previous Laboratory Results/Comments’ is now two separate fields, “Previous Laboratory Results” and “Comments”
When a test order with additional information or pre-approval requirement is selected, an information icon or
with alert pop-up window occurs.
“Specimen Source (Type)” is a required field and will be highlighted in red when not data is not entered.
Version and expiration date are updated: CDC 50.34 v2.0 (Expires December 8, 2017 at 11:59pm).