| Location: | Maryland |
|---|---|
| Posted: | Jun 23, 2026 |
| Due: | Jul 1, 2026 |
| Agency: | |
| Type of Government: | Federal |
| Category: |
|
| Solicitation No: | PANDHA-26-P-0000035401 |
| Publication URL: | To access bid details, please log in. |
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Office of Regulated Activities of the DHA R&D – Medical Research and Development Command (MRDC) has a requirement to manage, process, and complete initial labeling and labeling changes in electronic structured product label document submissions to the FDA. Structured Product Labeling (SPL) is a Health Level Seven (HL7) standard based on Clinical Document Architecture and HL7 Reference Information Model (RIM) accredited by the American National Standards Institute (ANSI) for the exchange of product information. The DHA R&D – MRDC currently has 2 licensed New Drug Application (NDA) products which require SPL submissions for up to 5 levels of primary and secondary labeling.
| May 15, 2026 | [Combined Synopsis/Solicitation (Original)] Structured Product Labeling (SPL) |
| May 20, 2026 | [Combined Synopsis/Solicitation (Updated)] Structured Product Labeling (SPL) HT9426-26-Q-E022 |
| Jun 5, 2026 | [Combined Synopsis/Solicitation (Updated)] Structured Product Labeling (SPL) HT9426-26-Q-E022 |
| Jun 11, 2026 | [Combined Synopsis/Solicitation (Updated)] Structured Product Labeling (SPL) HT9426-26-Q-E022 |
| Jun 29, 2026 | [Combined Synopsis/Solicitation (Updated)] Structured Product Labeling (SPL) HT9426-26-Q-E022 |

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