DRAFT - BCIS SOO.docx

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DRAFT Biological Containment Isolation System (BCIS)
Solicitation number
W911QY-26-S-BCIS-01
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This is a Statement of Objectives (SOO) for the Biological Containment Isolation System (BCIS), a prototype development effort issued by the U.S. Army Contracting Command-Aberdeen Proving Ground (ACC-APG), Natick Division. The SOO supports Call for Solutions Number W911QY-26-S-BCIS-01, issued under the Army Open Solicitation W9128Z-25-S-A002 via Broad Agency Announcement authority under 10 U.S.C. 4022. The Government intends to award multiple Prototype Other Transaction Agreements (OTAs) to offerors whose Solution Briefs are determined most advantageous based on evaluation criteria specified in the solicitation documents. Offerors must submit Solution Briefs addressing the objectives outlined in the SOO.

Inquiries and questions must be submitted via email to the Government Points of Contact no later than 1700 Eastern Time on 01 April 2026, with each offeror submitting only one consolidated set of questions. All communications concerning this competition must be directed exclusively to the identified Government POCs in writing, as unauthorized contact with other Government personnel may constitute an Organizational Conflict of Interest (OCI). The specific technical objectives and requirements for the BCIS prototype are detailed within the attached SOO document itself, which addresses the system's intended capabilities and performance parameters.

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CPE CBRND Industry Day_BCIS-PPTS-SIS_1-1 Attendeees_18MAR26.pdf PDF
Industry Day QA.xlsx XLSX spreadsheet
DRAFT Call for Solutions - BCIS .docx DOCX document
DRAFT - BCIS SOO.docx DOCX document
DRAFT Call for Solutions - BCIS .docx DOCX document

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STATEMENT OF OBJECTIVE (SOO)

DISTRIBUTION A. Authorized for public release, distribution unlimited.

PROJECT TITLE: Biological Containment Isolation System (BCIS)

BACKGROUND

The Capability Program Executive for Chemical, Biological, Radiological, and Nuclear Defense (CPE CBRND) and Joint Project Manager for CBRN Protection are seeking innovative biological containment, isolation, and quarantine (BIQ) capabilities for managing High-Consequence Infectious Disease (HCID) infected patients during contingency operations, in locations both in the Continental United States (CONUS) and Outside CONUS (OCONUS). The desire is for a negative pressure Multi-Patient BCIS tent / shelter. It is preferred that existing DoD tents /shelters be adapted to function in a negative pressure mode; however, other solutions will be considered. The BCIS will allow medical staff to monitor and/or treat patients while decreasing the risk of infecting other patients and staff.

ACQUISITION STRATEGY & OBJECTIVES

This Statement of Objectives (SOO) defines the goals for a multi-phased prototype project.

3.1 Acquisition Approach

Subject to the availability of funds, the Government intends to make multiple awards for prototype solutions. Up to three (3) contractors will be selected for Phase I. Following Phase I, the Government will conduct a down-selection to determine which contractors (up to two) will proceed to Phase II. An award to participate in Phase I is a prerequisite for consideration for Phase II.

To be considered successful and eligible for a non-competitive follow-on production award, a prototype must meet the following criteria.

Table 1: Minimum criteria for a successful prototype.

Requirement
Threshold
Force Protection
Negative pressure differential of 0.01 In.w.g

12 Air Changes per Hour (ACH)

99.97% at 0.3-micron particle diameter

System Interruption
Visual alarm when pressure is outside the required negative range
Patient Access
Anteroom allows personnel and litter-bound patient ingress/egress while maintaining negative pressure
Patient Movement
System accommodates movement of patients on standard litters (94” x 31”) while maintaining negative pressure
Power
Connects to and operates on standard military field power grid or its own integrated power source

Primary power sources must operate at normal temperature and pressure (20° C, 1 atm)

Reusability
System can be safely decontaminated and reused
Noise Level
≤ 75 dBA at operator position
Shelf Life
5 years
Environmental
No operational degradation from wind, rain, sand, or dust
EMI
Meets applicable MIL-STD-461
Transportation
Must demonstrate ability to be transported in stored configuration
Occupancy
Isolation room to accommodate at least 5 patients

3.2 Follow-on Production Authority

Upon successful completion of a prototype Other Transaction Authority (OTA) competitively awarded from this SOO, the Government may issue a follow-on production contract for up to 15 units without further competition, in accordance with 10 U.S.C. § 4022.

3.3 Proposal Requirements

Offerors shall use this SOO as the basis for their proposal. The proposal shall address the objectives of each phase for a multi-patient solution and include a draft Statement of Work (SOW) for the Government's consideration. Multiple SOW submissions per Offeror are acceptable.

This project is unclassified.

The proposal must contain the following distinct elements:

· A detailed master delivery schedule for all prototypes and data deliverables.

· The total firm-fixed-price for all prototypes and associated deliverables in each Phase.

· The Offeror's projected unit cost for a potential Full Rate Production (FRP) quantity.

· The Offeror's demonstrated or projected maximum monthly production rate.

· Supporting documentation to substantiate performance claims, including but not limited to: Technology Readiness Level (TRL) data, production lead times, test plans and reports, High Consequence Infectious Disease (HCID) containment data, analysis of interoperability with existing military field hospitals, power requirements, and durability data.

3.4 Phased Objectives

The following objectives apply to each phase. All requirements from Phase I carry forward and apply to Phase II, in addition to the new objectives listed for Phase II.

Phase I (One Prototype)

· Objective 1 (Delivery): The Contractor shall deliver one (1) prototype meeting a minimum TRL of six (6) to a Government-specified CONUS location.

· Objective 2 (Demonstration): At the specified location, the Contractor shall conduct a system demonstration of the prototype, covering setup, operational use (including containment), and breakdown procedures.

· Objective 3 (Evaluation): During the demonstration, Government and user personnel will conduct an assessment against the requirements and provide feedback. The Government will perform on-site confirmation of containment capabilities using Government-owned equipment. Upon completion of demonstration activities, the Government will transport the prototype to a designated facility for additional Government laboratory testing.

Phase II (Three Prototypes)

· Objective 4 (Delivery for Testing): The Contractor shall deliver three (3) prototypes meeting a minimum TRL of seven (7) to a Government-specified CONUS test facility.

· Objective 5 (Delivery for Demonstration): The Contractor shall deliver one (1) of the three prototypes to a Government-specified CONUS location for operational and logistics demonstrations.

· Objective 6 (Training and Support): The Contractor shall support an Initial Key Personnel Training (IKPT) event. Following this training, Government personnel will execute all operational and logistics demonstration vignettes using the Contractor-provided manuals. Upon completion of all Phase II activities, the Contractor shall transport the prototypes from the Government facilities.

SYSTEM (HARDWARE) DELIVERABLES

Specific delivery dates will be negotiated into the final SOW.

· Phase I: One (1) prototype system. The Government desires delivery within 60-90 days after award.

· Phase II: Three (3) prototype systems. The Government desires delivery within 60-90 days after Phase II start.

DATA DELIVERABLES

The Contractor shall deliver all data in formats to be negotiated and agreed upon with the Authorized Organizational Representative (AOR).

4.1 Start of Work Meeting & Minutes: Within 30 days of award, the Contractor shall host a Start of Work meeting to establish the project baseline, schedule, and risks. The Contractor shall deliver meeting minutes.

4.2 Test Support: The Contractor shall provide on-site technical support for test events as required. Assume two (2) travel days and two (2) days of support for each phase.

4.3 Schedule: The Contractor shall create, maintain, and execute against an Integrated Master Schedule (IMS).

4.4 Technical Data & Intellectual Property: The Government requires sufficient data rights to operate, maintain, and sustain the BCIS for its entire lifecycle.

Government Preference: The Government’s strong preference is for Unlimited Rights for all technical data, software, and associated intellectual property developed under this effort.

Offeror Assertions: The Offeror must include a table detailing any data rights assertions for technical data or software being provided with less than an unlimited/unrestricted license. This includes both commercial and non-commercial items. The Offeror must explain how this approach provides the best value to the Government over the system's lifecycle.

Evaluation Impact: The Government will evaluate the impact of any proposed data rights restrictions. Proposals that provide less than Government Purpose Rights (GPR) for the prototype design, or which hinder the competitive procurement of future sustainment services, may be evaluated negatively and could be a deciding factor in the selection decision.

4.5 Berry Amendment Compliance: The Contractor shall provide documentation verifying compliance with the Berry Amendment and detail the sourcing of any non-compliant items.

4.6 Safety Documentation: The Contractor shall deliver a Safety Assessment Report (SAR), Safety Data Sheets, and all necessary documentation for safe storage and disposal. At a minimum, the SAR shall summarize safety and health hazard data, provide a comprehensive evaluation of the safety and health risks, and identify procedures/precautions required for safe use of the system/subsystem and systems.

4.7 Manuals: The Contractor shall deliver all commercial or newly developed operator and maintenance manuals, updating them as the system baseline changes.

4.8 System Support Documentation: The Contractor shall deliver documentation specifying system size, weight, materials, equipment list, modes of operation, operating limits, and storage/transportation constraints.

PERIOD AND PLACE OF PERFORMANCE

The Contractor shall propose a delivery schedule in its SOW to include test support, technical readiness assessments, and other deliverables as outlined in Section 4.0. Prototype development will occur at the Contractor’s facility. Demonstrations and testing will occur at CONUS Government facilities designated after award.

AGREEMENTS OFFICER REPRESENTATIVE (AOR)

All communications and inquiries regarding this CFS shall be directed exclusively to the Agreements Officer.

· Agreements Officer: Dan L. Adams, Jr.

· Email: dan.l.adams2.civ@army.mil

ATTACHMENT 1 – PERFORMANCE REQUIREMENTS

The proposed solution should meet the Threshold requirements outlined in Table 2. Solutions exceeding Thresholds to meet Objective requirements are desired. The Government will consider partial solutions. The criteria in Table 3 will be used as additional considerations in the Government's best-value determination.

Table 2: Evaluation Criteria

Functional Area
Threshold
Objective
Verification Method
Negative Pressure
-2.5 Pa (≈ -0.01 in. w.g.) differential
-7.5 Pa (≈ -0.03 in. w.g.) differential
Government Test (GT) / Demonstration
Air Exchange Rate
12 Air Changes per Hour (ACH)
>12 ACH, not to exceed 25 ACH
Calculation based on enclosure volume and system airflow; confirmed via GT
Filtration Efficiency
99.97% removal of 0.3-micron particles
99.997% removal of 0.3-micron particles
GT in accordance with DOE-STD-3025-2022
System Interruption
Visual alarm when pressure is outside the required negative range
Visual and audible alarms
Demonstration
Patient Access
Anteroom allows personnel and litter-bound patient ingress/egress while maintaining negative pressure
Demonstration
Patient Movement
System accommodates movement of patients on standard litters (94” x 31”) while maintaining negative pressure
Demonstration
Power
Connects to and operates on standard military field power grid or its own integrated power source
Demonstration
Primary power sources must operate at normal temperature and pressure (20° C, 1 atm)
Demonstration
Reusability
System can be safely decontaminated and reused
Vendor Data / GT
Noise Level
≤ 75 dBA at operator position
< 70 dBA at operator position
GT in accordance with MIL-STD-1474
Shelf Life
5 years
> 5 years
Vendor Data / Analysis based on ASTM F1980
Environmental
No operational degradation from wind, rain, sand, or dust
GT in accordance with specified MIL-STD-810 methods
EMI
Meets applicable MIL-STD-461
GT / Certified Test Report
Transportation
Must demonstrate ability to be transported in stored configuration
Demonstration
Occupancy
Isolation room to accommodate at least 5 patients
Demonstration

Table 3: Additional Criteria

Factor
Evaluation Method
System Weight
Lower is more favorable.
Packaging
Smaller and lighter for transport is more favorable.
Setup Time
Less time is more favorable.
Setup Manpower
Fewer people are more favorable.
Procurement Cost
Lower evaluated price for prototypes is more favorable.
Sustainment Cost
Lower projected lifecycle cost is more favorable.
Producibility
Higher demonstrated production rate is more favorable.
Human Systems (HSI)
Favorable qualitative feedback and quantitative ratings from users.

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