Biological Containment Isolation System (BCIS)
Overview
Buyer
Place of Performance
NAICS
PSC
Set Aside
Original Source
Timeline
Qualification Details
Fit reasons
- NAICS alignment with historical contract wins in similar service areas.
- Scope strongly matches core technical capabilities and delivery model.
Risks
- Past performance thresholds may require one additional teaming partner.
- Potential clarification needed on staffing minimums before bid/no-bid.
Next steps
Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.
Quick Summary
The U.S. Army Contracting Command-Aberdeen Proving Ground (ACC-APG), on behalf of the Joint Project Manager for Chemical, Biological, Radiological, and Nuclear Protection (JPM CBRN P), is seeking prototype solutions for a Biological Containment Isolation System (BCIS). This system will convert existing USAF TMT60 positive-pressure tent shelters into negative-pressure, multi-patient isolation systems for managing High Consequence Infectious Diseases (HCID). This acquisition is conducted under 10 U.S.C. § 4022 Other Transaction Authority (OTA). Solution Briefs are due by June 23, 2026, 1700 EST.
Scope of Work
The Government requires a modular, field-installable kit to adapt the standard TMT60 tent. Key threshold requirements include maintaining a negative pressure of -2.5 Pa (≈ -0.01 in. w.g.), achieving ≥12 Air Changes per Hour (ACH), and 99.97% filtration efficiency for 0.3-micron particles. The solution must be compatible with and reversible for the TMT60 tent system. The effort is phased: Phase I involves developing TRL 6 prototypes, and Phase II advances to TRL 7.
Contract Details
This is a two-step acquisition intending to award multiple Prototype OTAs. Up to three contractors will be selected for Phase I, with a down-selection to up to two for Phase II. Successful completion of a prototype may lead to a non-competitive follow-on production contract for up to 15 units. The acquisition strategy encourages significant participation from non-traditional defense contractors and small businesses.
Submission & Evaluation
Step 1: Solution Briefs are required, consisting of a 15-page Solution Brief detailing technical merit, feasibility, and innovation, including a Rough Order of Magnitude (ROM) cost estimate, and a Supporting Data Package (no page limit). Submissions are via email to the listed Points of Contact. Step 2: Request for Solution Proposal (RSP) will be issued to selected offerors. Evaluation criteria for Solution Briefs include Threshold Assertions (Pass/Fail), OTA Eligibility (Pass/Fail), Technical Merit, and Programmatic Viability (ROM). Phase I evaluation considers Performance, Technical Maturity, Item Cost, and Risk Reduction. Final prototype selection (Phase II) will be based on Performance, User Feedback, and Affordability. The Government prefers Unlimited Rights for technical data and IP.
Key Requirements & Deliverables
Prototypes must meet specific performance thresholds: negative pressure (0.01 In.w.g.), ≥12 ACH, 99.97% filtration, visual alarms for pressure loss, anteroom for patient access, accommodation for standard litters, operation on military field power, reusability, ≤75 dBA noise, 5-year shelf life (filters)/10 years (non-filters), environmental resistance (MIL-STD 810H), EMI compliance (MIL-STD-461), transportability, and occupancy for at least 5 patients (two single-patient HCID units and four litters). Deliverables include prototypes (3 for Phase I, 5 for Phase II), master delivery schedules, projected unit costs for production, and supporting documentation.
Response Details
All Solution Brief packages must be submitted via email to Dan Adams (dan.l.adams2.civ@army.mil) and Andy Rhodes (andrew.r.rhodes10.civ@army.mil) by June 23, 2026, 1700 EST. Full details are in the attached CFS document.