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This Government Contract opportunity from Department Of Health And Human Services was posted on April 17, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Intent to sole source for BEST 1 Bridge Contract to Acumen LLC

Closed
FDAINTENTTOSOLESOURCEBRIDGECONTRACTBEST1Federal

Contract Overview

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

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NAICS: 541
Federal
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Solicitation # FA800325SC001
The Air Force Installation and Mission Support Center (AFIMSC) has established the Streamlining Procurement for Effective Execution and Delivery (SPEED) Commercial Solutions Opening (CSO) under solicitation FA800325SC001. This open, blanket CSO operates from September 1, 2025, to August 31, 2030, and is designed to facilitate the competitive procurement of innovative commercial items, technologies, and services. The program utilizes a multi-spiral solicitation process involving Area of Interest (AoI) calls, where the government seeks solutions such as the AFCEC Civil Engineer IT Portfolio Optimization to modernize IT systems, improve data quality, and enhance cybersecurity. Awards may be made as fixed-price contracts under FAR Part 12 or through Other Transaction Authority (OTA), with the government emphasizing the adoption of customary industry standards and the use of streamlined acquisition processes. Eligible participants include small businesses and non-traditional contractors who possess a Unique Entity ID and are registered in the System for Award Management. The evaluation process utilizes pass/fail gates based on the acceptability of the technical approach, the realism of the performance schedule, and the fairness of the proposed pricing. Offerors may submit initial proposals via a five-page written solution brief or a five-minute video. While the majority of work is expected to be performed at non-government facilities, some efforts may require access to DoD installations or networks. All submissions and inquiries are managed through the 772 ESS/Speed CSO and posted via SAM.gov.
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POSTED

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DEADLINE

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General Info

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant SvcsView Agency

NAICS

541

Place of Performance

Silver Spring, MD, 20993, USA

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

special-notice

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Contacts2 people available
OfficeRockville, MD, 20852, USA
Organization / Agency
Department Of Health And Human Services → FDA Office Of Acq Grant Svcs
View Agency Profile
Office AddressRockville, MD, 20852, USA

Full Description

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Intent to Award a Sole Source Contract:           4/17/2026


The purpose of this acquisition is to:
1. Ensure uninterrupted management and coordination of activities across the BEST distributed data network and multiple data partners.
2. Maintain analytic capacity and capabilities to run surveillance queries, generate population-based estimates, detect safety signals, and conduct follow-up analysis on detected safety signals across millions of person-records included in the databases of multiple data partners.
3. Avoid costly delays and/or disruptions in mission-critical operations by completing in-progress surveillance projects and requirements by federal law – i.e., fulfilling Congressional mandates from the FDA Amendments Act 2007, 21st Centuries Cures Act, and the Prescription Drug User Fee Act (PDUFA VII) – during the transition to Sentinel 3.0. The ongoing PDUFA demonstration project faces significant risk of missing critical regulatory timelines without immediate contract continuity measures.



Coordination of the BEST Initiative is a major component of the FDA’s active postmarket safety surveillance capabilities and is an essential and necessary part of the agency’s implementation of the 21st Century Cures Act and the FDA Amendments Act of 2007 to use electronic healthcare data to evaluate the safety and effectiveness of biologics. The Coordinating Center plays a central role in executing the BEST Initiative’s objectives by maintaining the data and analytical infrastructure, expertise, and partnerships needed to monitor, refine and identify  safety signals, inform regulatory decisions, and fulfill FDA’s statutory obligations for biologic product surveillance. 



This bridge action is a continuation of services currently being performed under IDIQ: HHSF223201810020I and Task Order: HHSF223201810020I / 75F40123F19005, awarded to Acumen, LLC, which serves as the BEST Coordinating Center. The current period of performance ends on 9/29/2026 with approximately $8,000,000.00 obligated to date.
The incumbent was competitively awarded the contract. The follow-on acquisition is already in progress, but due to procurement timelines, a limited-duration extension is necessary to prevent a lapse in service.



A sole-source bridge is being pursued because any transition of work to a new entity at this stage would introduce delays and inefficiencies, and such transition would also risk impacting system processes necessary for fulfilling FDA statutory obligations. The incumbent’s business systems including data infrastructure, analytical capabilities, staffing, data coordination, and communication processes are deeply embedded in ongoing projects. Restarting or onboarding a new contractor would result in duplicative costs, loss of institutional knowledge, and disruption to time-sensitive public health surveillance deliverables.



This contract supports the coordinating center for the Biologics Effectiveness and Safety (BEST) Initiative. The coordinating center serves as the central hub for managing all aspects of the program, including the administration of task orders, coordination of data partners, project tracking, timeline oversight, and quality control across active surveillance activities. The coordinating center provides program management, technical infrastructure, analytical capabilities, scientific support, and administrative oversight to ensure the timely and consistent execution of surveillance studies conducted through separate contracts with data partners.



All work is governed by the Statement of Work and organized into infrastructure and study-related tasks. The coordinating center ensures continuity across projects, supports knowledge management, and maintains the technical infrastructure needed to support standardized data transformation and querying through the common data model, enabling timely and efficient delivery of safety surveillance outputs to meet CBER’s regulatory needs.



The 12 month bridge contract is required to ensure effective continuity of operations to protect Public Health from 9/30/2026 – 09/29/2027 for a total contract value approximately of $6M.

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The U.S. Food and Drug Administration, through the Center for Drug Evaluation and Research, intends to award a sole-source, firm-fixed-price purchase order to OrganoTherapeutics SARL for human iPSC-derived hindbrain organoid functional assay services. This acquisition, conducted under FAR Part 12 as a commercial service, aims to support in vitro research on drug-induced effects on respiratory-relevant neural circuits. The scope of work includes the provision of human hindbrain organoids and associated culture materials, with twelve scheduled deliveries to the FDA White Oak Campus in Silver Spring, Maryland. The first delivery will consist of 96 organoids, followed by eleven subsequent deliveries of 48 organoids each. The contractor will perform functional characterization at its own laboratory using three-dimensional multi-electrode array technology to assess electrophysiological responses to FDA-identified drug and reversal-agent combinations. Key deliverables include the raw and analyzed data, analysis files, and comprehensive study reports. The anticipated period of performance is 18 months from the date of award. Award will be based on best value, with technical capability and past performance weighted more heavily than price. All invoicing must be processed electronically through the U.S. Department of Treasury's Invoice Processing Platform.
Research and Development in Biotechnology (except Nanobiotechnology)

POSTED

about 20 hours ago

DEADLINE

in 5 days
View Details

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