October 21, 2026
FASTPASS ISO, ARPA-H-SOL-26-160, Amendment 01
The purpose of Amendment 01 is to:
(1) Revise Section 1.2 of the Appendix C.3: Cost Proposal Narrative Model;
(2) Rename Attachment D: Cost Proposal Workbook to Appendix D: Cost Proposal Workbook; and
(3) Revise item 4 under the General tab of Appendix D: Cost Proposal Workbook to correct a typographical error.
No other changes were made to the body of the ISO or appendices.
See attached FASTPASS ISO, ARPA-H-SOL-26-160, Amendment 01.
August 20, 2026
The Advanced Research Projects Agency for Health (ARPA-H) Fast Assessment of Solutions, Therapeutics, Pharmaceuticals, and SupplieS (FASTPASS) program aims to develop a near real-time, non-destructive, AI-enabled system for screening pharmaceutical products and inputs through their packaging at ports of entry and other supply-chain nodes.
Interested parties are invited to review the attached FASTPASS Innovative Solutions Opening, ARPA-H-SOL-26-160.
The FASTPASS program aims to develop and demonstrate a near real-time, non-destructive, through-packaging, AI/ML-enabled testing and quality monitoring system for pharmaceutical products and their inputs. The program is structured around two technical areas: TA1 for next-generation, fieldable sensing technologies (e.g., nuclear magnetic/quadrupole resonance, spatially offset Raman spectroscopy, time-domain terahertz spectroscopy, x-ray fluorescence, x-ray diffraction, hyperspectral approaches) and TA2 for computational models and integrated system software that can interpret weak, noisy, heterogeneous signals under real-world conditions. The program is divided into three 18-month phases, with performers evaluated through increasingly realistic demonstrations, moving from component-level performance to rugged, transportable prototypes capable of rapid screening with extremely low false-alarm rates. The system must be able to screen pharmaceutical products through six major packaging types: boxes of liquid vials or syringes, bottles of solid oral dosage forms, boxes of lyophilized vials, boxed blister packs, boxed liquid solutions in bags, and barrels of bulk powdered ingredients. The goal is to enable rapid, mobile, field-deployable screening at import points of entry and other critical supply-chain nodes.
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A surety’s written statement that it expects to bond you up to a stated amount, subject to final underwriting. It’s what an agency asks to see before they take your bid seriously.
Source: SAM.gov (notice 1479442e64d740b59cc92c717bd329bc), retrieved via the SAM.gov Get Opportunities API. View the official posting, and always confirm requirements and deadlines with the issuing agency.