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VA Technical Reference Model v 24.4

Medi-Dose Information Labeling Technology (MILT)
Medi-Dose Information Labeling Technology (MILT) Technology

General InformationGeneral Information help

Technologies must be operated and maintained in accordance with Federal and Department security and privacy policies and guidelines. More information on the proper use of the TRM can be found on the TRM Proper Use Tab/Section.

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Description: Medi-Dose Information Labeling Technology (MILT) provides capabilities for the design, printing, and reporting of labels and the packaging of unit dose medications. MILT supports all standard types of bar codes. The technology allows users to customize labels with information such as National Drug Codes (NDC), lot numbers, beyond-use dates, hospital codes, wholesaler numbers, and identification codes. Each label printed is recorded in an electronic log that creates a report to manage packaged labels.

This technology does not utilize a database, as files generated by this technology are saved to the user`s local drive and may be shared with other users over a local network.

For printing purposes, MILT is compatible with both standard laser printers and Zebra thermal printers, including the Zebra LP-2844/GK420d/GC420d Direct Thermal Printer.
Technology/Standard Usage Requirements: Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 6102 and 6500; VA Directives 6004, 6513, and 6517; and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS). Users must ensure sensitive data is properly protected in compliance with all VA regulations. Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation.
Section 508 Information: This technology has been assessed by the Section 508 Office and found non-conformant. The Implementer of this technology has the responsibility to ensure the version deployed is 508-compliant. Section 508 compliance may be reviewed by the Section 508 Office and appropriate remedial action required if necessary. For additional information or assistance regarding Section 508, please contact the Section 508 Office at Please see reference tab for more information concerning product versions.
Decision: View Decisions

Decision Source: TRM Mgmt Group
Decision Process: One-VA TRM v22.11
Decision Date: 11/04/2022 at 01:37:21 UTC
Introduced By: TRM Request
Vendor Name: Medi-Dose/EPS
- The information contained on this page is accurate as of the Decision Date (11/04/2022 at 01:37:21 UTC).