Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, October 28 at 2:00 PM ET

Register Free →

This Sources Sought opportunity from Department Of Defense was posted on June 2, 2021. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Needle-free mRNA Vaccine Delivery System

Closed
W911QY-21-S-0007Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

Active Opportunities Like This One

NAICS: 541715
New
Federal
U.S. Army Contracting Command – Watervliet Arsenal (ACC-WVA) Organic Industrial Base (OIB) Modernization Commercial Solutions Opening (CSO)
Solicitation # W911PT26SC001
The U.S. Army Contracting Command – Watervliet Arsenal (ACC-WVA) has issued solicitation W911PT26SC001, a Commercial Solutions Opening (CSO) authorized under the National Defense Authorization Act for Fiscal Year 2026 and DFARS Subpart 212.70. This competitive solicitation is open until September 30, 2027, and is designed to acquire innovative commercial products, technologies, and services to modernize the Army's Organic Industrial Base. The scope focuses on integrating manufacturing resources, linking legacy analogue systems with digital systems, and expanding modeling and simulation to enhance the delivery of materiel solutions. The CSO targets both traditional and non-traditional business entities, including small businesses and foreign-owned firms, provided they maintain an active System for Award Management (SAM) profile and a Unique Entity ID. The acquisition process follows a multi-phased approach consisting of a written solution brief, an optional presentation or pitch, and a final Request for Commercial Solution Proposal (CSP). Evaluation is based on responsiveness, technical merit, uniqueness, and price reasonableness. Successful responses may result in fixed-price contracts awarded under FAR Part 12 Commercial Item Procedures. Current Areas of Interest (AoIs) include advanced cannon technology, electrical infrastructure improvements at Building 120, chromium facility conversion, automated manufacturing for minor components, automated cooling tower treatments, advanced CNC vertical turning lathes, and advanced tooling for radial forging. Performance is primarily located at Watervliet Arsenal and Benet Laboratories, with a general period of performance not to exceed 12 months unless otherwise specified.
W6QK Acc Wva

POSTED

about 7 hours ago

DEADLINE

in 12 months

General Info

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Place of Performance

MA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

AI Contract Breakdown

Uniform Contract Format

No documents to break down

The breakdown needs solicitation documents. None were found from this contract's source.

Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

Find active opportunities like this

Start your free trial to discover similar active contracts, track opportunities, and build proposals with AI assistance.

Organization & Contact Information

Show more
AgencyDepartment Of Defense → W6QK Acc-Apg Natick
Contacts1 person available
OfficeNATICK, MA, 01760-5011, USA
Office AddressNATICK, MA, 01760-5011, USA

Full Description

Show more
W911QY-21-S-0007 REQUEST FOR INFORMATION Needle-free mRNA Vaccine Delivery System Objective: This is a Request for Information (RFI) for planning purposes only. It is not to be construed as a commitment by the Government nor will the Government pay for the information solicited. No solicitation document exists or is guaranteed to be issued as a result of this RFI. The Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO CBRND) is seeking information on the capabilities and willingness of private entities (academic, non-profit and commercial) to design, test, manufacture, and serve as regulatory sponsor for an mRNA vaccine delivered by mechanisms other than traditional needle and syringe. Needle-free vaccine delivery technologies for consideration should ideally be easy to manufacture, transport, and store, and should be easy to administer/enable self-administration (example technologies include transdermal microneedle patches, oral formulations, aerosol formulations). A list of potential mRNA vaccine targets that the Government is interested in is provided in Appendix 1 below. The Government is requesting information on the following: Design, development, manufacturing using current Good Manufacturing Practices (cGMP), and lot release and stability testing of alternative non-traditional delivery techniques for mRNA vaccine delivery Formulation and stabilization of an mRNA construct for delivery via vaccine skin patch or alternative delivery techniques Utilization of alternative delivery techniques to elicit protective immune responses with a single dose and/or reduce cold-chain requirements Preclinical efficacy and safety testing of alternative needle-free vaccine delivery methods Regulatory sponsorship and execution of human clinical trials for safety, immunogenicity, and efficacy (if available) testing, and potential FDA Animal Rule development pathway Background: JPEO CBRND is seeking information on capabilities for the development of a needle-free mRNA vaccine delivery system outlined in the objectives above. Executing this objective may include leveraging existing relationships between industry and academia, leveraging previously FDA-approved mRNA-based vaccine technologies, as well as leveraging any existing partnerships to satisfy FDA regulatory requirements necessary for future human safety and efficacy testing. Requirements: The purpose of this RFI is to request information on the ability to develop, manufacture, and test a needle-free method for the effective delivery of mRNA vaccines. JPEO CBRND would like to understand industry's ability to: design and develop a needle-free method for effective immunization; formulate and/or stabilize mRNA vaccines for needle-free delivery; and test the vaccine and needle-free delivery method separately and in combination to demonstrate safe and effective vaccine delivery through preclinical studies and human clinical trials. Administration: The Government will retain comments and information received in response to this RFI. Proprietary information should be identified as Company Proprietary. Do not use Government security classification markings. All written responses must be received by COB on 2 Jul 2021. Responses should be sent by e-mail to: usarmy.detrick.jpeo-cbd.mbx.mcs-rfi@mail.mil, with Subject Line of Responding Organization and RFI Title. Material that is advertisement only in nature is not desired. If a solicitation is subsequently released based on the responses to this RFI the first choice for an acquisition vehicle, if appropriate, will be the Medical CBRN Defense Consortium (MCDC) Other Transaction Agreement (OTA). Respondents not already members of the consortium are encouraged to join at www.medcbrn.org. Respondents may also inquire about the MCDC at mcdc@ati.org. Performance Objectives: When responding to this RFI, please provide responses to the objectives listed limited to 10 pages. Responses submitted should also include answers to all of the following prompts: Design, development, manufacturing, and testing of needle-free vaccine delivery system Describe existing capability to design needle-free methods for vaccine delivery Design considerations and existing or planned testing of needle-free delivery method with/without mRNA vaccine Vaccine construct(s) tested with the needle-free design Describe existing or planned capability to manufacture mRNA vaccine delivery needle-free methods suitable for human use. Please address: Expected throughput and ability to scale up production Quality control and cGMP manufacturing mRNA vaccine formulation for needle-free delivery Describe existing capability to formulate and test mRNA vaccines for needle-free delivery. Please address: Product storage and transport conditions Product stability (time, temperature and any other requirements) Product stability testing considerations Describe experience in manufacturing and releasing sufficient quantities of cGMP material for Phase I-III human clinical trials Describe any current collaborations/partnerships with entities currently manufacturing clinical lots of mRNA vaccines for use in formulation studies Preclinical testing of vaccine needle-free delivery system safety and efficacy Describe experience in performing preclinical testing for U.S. regulatory applications Describe any current collaborations/partnerships with entities experienced in the design and conduct of preclinical studies for U.S. regulatory applications Regulatory sponsorship and execution of human clinical trials for safety and efficacy testing and/or FDA Animal Rule clinical trials where necessary Describe experience in serving as regulatory sponsor and obtaining FDA product approval(s) Appendix 1. Biological Threat List The Government interested in potential capabilities to address the following CBRN, pandemic influenza, and emerging infectious disease threats: Virus targets Filoviruses Pandemic influenza (H5 and H7 specifically) Alphaviruses Flaviviruses (Zika virus specifically) Arenaviruses Bunyaviruses Bacterial Plague Tularemia Melioidosis Glanders Q Fever Toxin threats Botulinum toxin Ricin Conotoxins Saxotoxins

More opportunities from Department Of Defense → W6QK Acc-Apg Natick

Same awarding agency

NAICS: 541380
New
Federal
Chemical Nutrient Analysis Service for Combat Feeding Division (CFD)
Solicitation # W911QY-26-R-NUTRIENT-ANALYSIS
The U.S. Army Contracting Command Aberdeen Proving Ground, Natick Division, is soliciting proposals for chemical nutrient analysis services to support the Combat Feeding Division of the U.S. Army Combat Capabilities Development Command Soldier Center. The requirement involves outsourcing the nutritional analysis of food ingredients and ration components, with a primary focus on selenium, vitamin B12, and total dietary fiber, though the contractor must be capable of analyzing all analytes listed in the statement of work. This is a full and open competition under NAICS code 541380, intended to be awarded as a single Indefinite Delivery Indefinite Quantity IDIQ, Firm Fixed Price contract. The contract features a minimum guarantee of 5,000 dollars and a maximum ceiling of 25,000 dollars, with an anticipated period of performance from November 1, 2026, to October 31, 2027. Eligible offerors must be registered in the System for Award Management and maintain active ISO/IEC 17025 accreditation for the duration of the contract. All testing must utilize validated industry standard methods, such as AOAC International, USP, or AACC, and be performed using in house capacity rather than through pass through arrangements. Key deliverables include data reports submitted within 14 calendar days of sample receipt and the maintenance of a documented chain of custody. Proposals will be evaluated based on technical capability, price, and past performance, with the award going to the responsible vendor representing the Lowest Price Technically Acceptable offer. Submissions must be divided into separate technical and pricing proposals and delivered by 12:00 p.m. EST on October 29, 2026.
Testing Laboratories and Services

POSTED

4 days ago

DEADLINE

in 9 days
View Details
NAICS: 315120
New
Federal
Request for Information on Combat Boot Sock
Solicitation # RequestForInformationOnCombatBootSock
The U.S. Marine Corps Portfolio Acquisition Executive Marine Corps is conducting market research through a Sources Sought Announcement to identify potential manufacturers for a high-performance combat boot sock. Designed for Department of Defense personnel operating in temperatures above 20 degrees Fahrenheit, the socks must be Berry Amendment compliant domestic productions. The required design is an over-the-calf length featuring cushioning to prevent blisters, graduated compression to promote blood flow, a non-slip top cuff, arch support, and nylon reinforcement at the heel and toe. Material specifications require a minimum of 52 percent wool (25 microns or finer), 20 percent nylon, and 1 percent spandex, with a strict prohibition on cotton and rayon fibers. The socks will be required in four classes: Marine olive drab green, black, coyote 498, and undyed/natural, across sizes small through extra-large. Performance standards include strict criteria for bursting strength, dimensional stability, wicking, and colorfastness, with quality inspections following ASTM D3990 and ASQ/ANSI Z1 standards. This is currently a Request for Information for planning purposes only and does not constitute a solicitation or commitment to procure. Interested parties, including non-manufacturing suppliers with qualified domestic partners, must submit their CAGE code, business size, and NAICS information electronically to the designated points of contact by October 30, 2026, at 5:00 PM EST.
Apparel Knitting Mills

POSTED

4 days ago

DEADLINE

in 10 days
View Details
NAICS: 541990
New
Federal
Request for Information (RFI) - Medical Fielding Short-Term
Solicitation # RFI_MedicalFieldingShortTermNov2026
The US Army Medical Materiel Development Activity is issuing a Request for Information for short-term Materiel Fielding and Medical Liaison Support Services to support the Program Executive Office Soldier and Project Manager Soldier Medical Devices. The government seeks to identify capable contractors for a three-month engagement running from November 3, 2026, to February 2, 2027. The scope of work includes the procurement, assembly, distribution, and disassembly of medical equipment and materiel sets, kits, and outfits. Key deliverables include monthly metrics reports, the execution of medical screenings via DD 2795 Pre-deployment Health Assessments, and the establishment of a classified, secured warehouse facility within the continental United States. Performance will occur at both CONUS and OCONUS locations, including sites in Maryland, Alaska, and Germany, requiring compliance with the U.S. ROK SOFA agreement. Due to the nature of the work, the contractor must possess a facilities clearance, and multiple positions require Secret clearances. Additionally, the contractor must act as a Business Associate under HIPAA regulations, ensuring all personnel complete annual privacy and security training. Other critical requirements include the submission of Organizational Conflict of Interest certifications, adherence to non-disclosure agreements, and completion of Hazard Material Handler Safety Courses. Interested respondents must submit a white paper limited to five pages by October 21, 2026, detailing their capabilities and addressing specific concerns in section 2c of the PWS. This request is for informational purposes under FAR part 16.505 and does not constitute a formal solicitation or a commitment to award a contract.
All Other Professional, Scientific, and Technical Services

POSTED

5 days ago

DEADLINE

in about 19 hours
View Details

Find Active Opportunities Like This

Get AI-powered intelligence on the opportunities still open

Every page of the solicitation package shredded into a compliance breakdown

AI-powered matching based on your capabilities and past performance

Competitor and incumbent history on the requirement

Automated alerts on amendments, Q&A deadlines, and award

Miguel
Hillary
Keith Deutsch
Christine

Join 750+ contractors already using CLEATUS