75D30124Q77727_QandA.docx
DOCX document 16 KB Posted
- Attached to
- Pre- and Post- Influenza Human Sera Panels Federal contract opportunity
- Solicitation number
- 75D30124Q77727
About this file
This document is a set of Questions and Answers (Q&A) related to Solicitation # 75D30124Q77727 for Pre- and Post-Influenza Human Sera Panels. The solicitation is seeking the provision of anonymous serum samples from six age cohorts to test for vaccine-induced antibodies against newly circulating influenza virus strains.
The Q&A addresses one key question regarding the type of influenza vaccine that can be used for the young pediatric participants (ages 6 months to 35 months) if the current licensed trivalent seasonal egg-based influenza vaccine is not available. The answer states that the cell-based influenza vaccine is acceptable and the preferred vaccine for the base year. Larger volume serum samples from some adult participants are also required for further testing.
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Other files for this federal contract opportunity
| File | Type | Posted |
|---|---|---|
| Amendment_00001_RFQ_75D30124Q777727.pdf | ||
| A19_SF1449 - POST.docx | DOCX document | |
| A19_Combined SynSol_Post_Final.docx | DOCX document |
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Pre and post Influenza Human Sera Panels Solicitation # 75D30124Q77727 Questions
1. If the current licensed trivalent seasonal egg-based influenza vaccine is not available to meet the necessary first year timeline, what other vaccines will be acceptable for the young pediatric participants (age 6 months to 35 months)?
ANSWER: Page 18 of the solicitation states that, “This cohort must receive the current licensed seasonal cell-based and /or egg-based influenza vaccine, or other vaccine type as specified by CDC.” The cell-based influenza vaccine is available for 6 month - 35 months pediatric participants and is acceptable. This is the vaccine that will need to be used and is the preferred vaccine in the base year.
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