Name | Type | Posted | Actions |
|---|---|---|---|
RFP 75A50121R00013 Pages 1-2 9-10-2021.pdf | Sep 10, 2021 | ||
Amendment 4 - Summary.pdf | Sep 10, 2021 | ||
RFP SOW-New Stockpile Updated with Responses 9-2-2021.pdf | Sep 3, 2021 | ||
New Email Account 8-29-2021.pdf | Aug 29, 2021 | ||
Amendment 3 - Past Performance Update v1.pdf | Aug 26, 2021 | ||
Amendment 3 - Past Performance Update.pdf | Aug 25, 2021 | ||
Response - Proposal Ext.pdf | Aug 18, 2021 | ||
QA for Follow-On Stockpile - Additional Questions - 8-16-21 FINAL .pdf | Aug 17, 2021 | ||
QA for Follow Stockpile - IDIQ 8-6-21 FINAL.pdf | Aug 7, 2021 | ||
Amendment 2 - Summary.docx | DOCX | Jul 26, 2021 | |
RFP SOW-New Stockpile 6-29-2021 - Amendment 1.pdf | Jul 23, 2021 | ||
Amendment 1 - Summary.pdf | Jul 23, 2021 | ||
RFP SOW-New Stockpile 6-29-2021 - Program Updated - CLEAN.pdf | Jun 29, 2021 |
Acquisition of Medical Countermeasures (MCMs) for Pandemic Influenza and Emerging Diseases Preparedness and Response
Contact and place of performance
Wendell Conyers
DC
USA
Reference Amendment 1 PERIOD OF PERFORMANCE a. The base period of performance of this contract is anticipated for thirty-six (36) monthsfrom date of award. The period of performance may be extended up to 24 months withthe exercise of option(s), structured as CLINs. b. If the Government exercises its option(s), the period of performance will be increased as listed below: Option I Twelve (12) Months (Year 4) Option II...
View moreThe Office of the Assistant Secretary for Preparedness and Response, specifically the BARDA Division of Contracts Management and Acquisition, issued solicitation 75A50121R00013 for the manufacturing and maintenance of influenza vaccines and adjuvants. This combined synopsis/solicitation falls under NAICS 325414 for Biological Product (except Diagnostic) Manufacturing and PSC 6505 for Drugs and Biologicals. The primary scope includes the production of cGMP influenza vaccine master and working seed lots, research and investigational lots, commercial-scale bulk lots, and adjuvants that have completed Phase 2 development. Services also encompass formulation and filling, candidate vaccine virus development, storage and stability testing, and disposal of product.
The anticipated period of performance consists of a 36-month base period starting from the date of award, with two 12-month options that could extend the total duration to 60 months. The minimum guarantee for any resultant contract is $50,000.00. Contractors are required to provide firm-fixed pricing for most contract line items, though specific tasks related to shipping, clinical and non-clinical studies, analytical laboratory testing, and emerging pathogen response will be determined through subsequent Requests for Task Order Response. Performance is located in Washington, DC, and the response deadline is September 13, 2021.
The procurement process is managed by Wendell Conyers and includes 13 attachments such as the Statement of Work, multiple amendments, and specific reporting requirements. Notable requirements include the provision of yield-optimized seed lots for inactivated, live attenuated, or recombinant products, as well as clinical evidence of antigen sparing or adjuvant benefit for proposed adjuvant bulk products. The contract also accounts for the storage and stability of materials produced under prior contracts and mandates standard data reporting for all activities.
Generated by Lumen AI
Scoped analysis and attachments—go beyond the summary when you need detail from the solicitation package.