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FISHER BIOSERVICES INC 14665 ROTHGEB DRIVE Rockville MD 20850 USA

UEI: SLED_C454C135FD24FCB3

FISHER BIOSERVICES INC 14665 ROTHGEB DRIVE Rockville MD 20850 USA is a federal contractor, registered under UEI SLED_C454C135FD24FCB3. It has been awarded $100,000,000 across 1 federal contract. Primary work spans Research and Development in Biotechnology (except Nanobiotechnology). Top awarding agencies include National Institutes Of Health Nichd.

Contact Information

Registration and classification details

Registration

UEI Code

SLED_C454C135FD24FCB3

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

Key Performance Metrics

Awards Count

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Award Analytics & Distribution

Awards by Agency

National Institutes Of Health Nichd$100.0M100%

Awards by NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)$100.0M100%

Awards by Agency Over Time

Awards by Place of Performance

Open opportunities in FISHER BIOSERVICES INC 14665 ROTHGEB DRIVE Rockville MD 20850 USA's top NAICS codes and agencies

Humanized Antibody Library Screening and Transferrin Receptor DevelopmentThe contract involves the customized screening of a humanized antibody library to develop a functional transferrin receptor, encompassing molecular design, in vitro selection, and optimization of binding affinity and specificity. The work requires advanced techniques in antibody engineering to identify and refine candidates capable of high-affinity, selective interaction with the transferrin receptor, with the goal of producing a therapeutically viable candidate. The scope includes iterative cycles of library screening, functional characterization, and structural optimization to enhance target binding while minimizing off-target interactions, ensuring the final product meets stringent performance benchmarks. This subcontract is issued under the NAICS code 541714 for research and development in the biological sciences and is associated with the National Institutes of Health through the Department of Health and Human Services. The place of performance is in Bethesda, Maryland, with a deadline for proposals set for July 31, 2026. The contract is expected to support biomedical innovation targeting receptor-mediated delivery systems and requires expertise in molecular biology, high-throughput screening, and protein engineering. No specific set-aside provisions are indicated, and the work is open to qualified subcontractors capable of delivering scalable, data-driven antibody development solutions within the defined timeline.

National Institutes Of Health Olao

POSTED

DEADLINE

Recombinant Antibody Discovery & Engineering ServicesThe contract involves the discovery, humanization, and engineering of single domain antibodies designed to penetrate the blood-brain barrier using phage and yeast display platforms. This effort includes advanced antibody optimization through affinity maturation to enhance binding strength and specificity, as well as comprehensive stability testing to ensure functional integrity under physiological conditions. The work is scientifically focused on developing recombinant antibody formats capable of crossing the blood-brain barrier, a critical step for therapeutic applications targeting neurological diseases. This subcontract, issued by the National Institutes of Health under the Department of Health and Human Services, is classified under NAICS code 541714 for research and development in the physical, engineering, and life sciences. The opportunity was posted on July 24, 2026, with a response deadline of August 3, 2026. Performance is expected to take place in Bethesda, Maryland, 20892. The project does not specify a set-aside type or point of contact details, and the full solicitation can be accessed via the provided SAM.gov link for additional procedural or submission guidelines.

National Institutes Of Health Olao

POSTED

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Bioinformatics and Data Analysis for Biomarker ResearchThe contract titled Bioinformatics and Data Analysis for Biomarker Research seeks to deliver computational analysis of high-throughput sequencing data with the goal of identifying and validating biomarker signatures, accompanied by the generation of detailed research reports. This effort is classified as a subcontract under NAICS code 541714 and is managed by the Department of Veterans Affairs through its 245-NETWORK Contract Office 5. The work is to be performed at a location in Washington, D.C., with a zip code of 20422. The opportunity was posted on July 24, 2026, and responses are due by August 7, 2026, at 5:00 PM EST. Although no specific set-aside designation is indicated, the contract is structured to support advanced bioinformatics capabilities essential for translational research in biomarker discovery.

245-NETWORK Contract Office 5 (36C245)

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Develop and Validate Transferrin ReceptorThe National Institutes of Health, under the Department of Health and Human Services, has issued a presolicitation notice for the development and validation of a transferrin receptor, identified by solicitation number 75N98026Q00866. This opportunity is open for responses until July 31, 2026, and was posted on July 24, 2026, with no set-aside provisions applied, making it open to all eligible entities. The work will be performed in Bethesda, Maryland, and falls under the NAICS code 541714, which corresponds to research and development in the physical, engineering, and life sciences. The primary point of contact for inquiries is Towanda Daniels, reachable via email at danielt@mail.nih.gov. Interested parties are directed to the official SAM.gov workspace link for further details and submission guidelines. The contract aims to support advanced scientific research focused on the transferrin receptor, likely to advance biomedical applications or therapeutic technologies. All proposals must adhere to the requirements outlined in the notice of intent, and submissions should be prepared with consideration for the technical scope, timeline, and performance standards expected by the NIH Office of Laboratory Animal Welfare. The contract is structured to enable innovation in molecular biology or drug delivery systems involving receptor targeting, with performance expected within the confines of federal research protocols and compliance standards.

National Institutes Of Health Olao

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Humanized single domain antibodies for therapeutic brain deliveryThe National Institutes of Health Office of Extramural Research, under the Department of Health and Human Services, has issued a presolicitation for the development of humanized single domain antibodies designed for therapeutic delivery across the blood-brain barrier. The project, identified by solicitation number 75N98026Q00867, aims to advance novel antibody technologies capable of targeting brain-specific pathologies with enhanced precision and efficacy. All responses are due by August 3, 2026, and no set-aside provisions are applicable, meaning the opportunity is open to all eligible entities. The performance location is designated as Bethesda, Maryland, with the contract administration handled by the agency’s office at 20892. Primary point of contact for inquiries is Towanda Daniels, reachable via email at danielt@mail.nih.gov. The solicitation was posted on July 24, 2026, and all potential offerors are directed to the designated SAM.gov workspace for additional details and documentation. No NAICS code has been assigned at this stage, and the initiative reflects a strategic effort to enable breakthrough treatments for neurological disorders through innovative biotherapeutic platforms. Applicants must ensure full compliance with the requirements outlined in the attached Notice of Intent.

National Institutes Of Health Olao

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Notice of Intent to Award a Sole Source Contract – Sequencing Bundibugyo virus disease (BDBV) in the 2026 outbreakThe Food and Drug Administration is planning to award a sole source firm-fixed price purchase order to The University of Liverpool under simplified acquisition procedures for the sequencing of Bundibugyo virus disease during the 2026 outbreak, relying on FAR Part 6.103-1 which permits non-competitive procurement when only one responsible source exists. This action falls under the NAICS code 541714 for Research and Development in Biotechnology and is not open for competitive bidding, as the FDA has determined that The University of Liverpool is the only entity with the necessary expertise and capacity to meet the technical requirements for this highly specific viral sequencing effort. The contract is intended to support bioanalytical method development and sample analysis by providing critical reagents and reference standards for quantifying CYP enzyme substrates and metabolites in hepatocyte experiments during the outbreak response. Responses to this notice must be submitted by Ryan Alexander at ryan.alexander@fda.hhs.gov no later than 5:00 pm on July 29, 2026, and must include a detailed capability statement for any other organization seeking consideration, though the government retains full discretion to determine whether a response justifies competitive solicitation. The procurement is not a request for competitive quotes, and no set-aside is being applied. The contract will be administered from the FDA’s office in Rockville, Maryland, with performance primarily occurring in Liverpool, England, and the solicitation number is OC-2026-135667, issued on July 24, 2026.

Food And Drug Administration

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Procurement of lateral flow (LFA) strips for the rapid HIV nucleic acid diagnostic testThe Centers for Disease Control and Prevention is soliciting bids for the procurement of 4,000 lateral flow strips intended for use in a rapid HIV nucleic acid diagnostic test under a firm-fixed-price contract, issued as a Request for Quote in accordance with FAR Subpart 12 for commercial items. The solicitation number is 75D30126Q79099, with a performance period of August 1, 2026, to December 31, 2026, and an option to extend services for up to six additional months. Proposals must be submitted electronically to Eugene Gutierrez at zvm0@cdc.gov no later than 3:00 P.M. Eastern Standard Time on Friday, July 24, 2026, with no telephonic or paper submissions accepted. The place of performance is the CDC facility at 1600 Clifton Road, Building 17, Atlanta, GA 30329-4018. Offerors must be registered in the System for Award Management at the time of submission and are required to comply with all applicable FAR clauses, including 52.212-1 and 52.212-4, along with deviations such as those addressing trafficking in persons, contractor employee whistleblower rights, sustainable products and services, Buy American Act alternatives for Israeli and Korean end products, and prohibitions on unauthorized information sharing. Technical evaluation is the predominant factor in award, emphasizing experience with biomedical devices, FDA approval processes, and prior work with lateral flow technology, with price considered secondary. The contractor must deliver 200 prototype strips and 4,000 final units meeting stringent performance standards: ≤0.5% false positive rate and ≤1% false negative rate using CDC’s LAMP reaction, and must ensure full compatibility with CDC’s mass production protocols. All deliverables must conform to Section 508 accessibility requirements, including WCAG 2.0 Level AA, and vendors must provide a Voluntary Product Accessibility Template or HHS conformance checklist. The contract imposes strict security and confidentiality obligations, including mandatory non-disclosure agreements for all employees accessing sensitive information, identification protocols to distinguish contractor personnel from government staff, and prohibitions against retaining or disseminating federal records or Privacy Act data. Subcontractors must be bound by the same requirements, and all payments must be processed via the Treasury’s Invoice Processing Platform using an ACH Vendor Enrollment

CDC Office Of Acquisition Services

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Illumina Reagent KitsThe United States Department of the Naval Medical Research Command intends to award a sole source contract to Illumina, Inc. of San Diego, California, for the purchase of Illumina Reagent Kits. This procurement is not a competitive solicitation, but responses received will be considered if submitted. The action is classified under NAICS code 541714 and will be conducted under FAR Part 12 guidelines for commercial items. All vendors must be registered in the Systems for Award Management (SAM) and possess a Unique Entity Identification Number (UEI) to be eligible for award, with SAM registration available free of charge through sam.gov or by calling (866) 606-8220. The contract is identified by solicitation number 1301397256, posted on July 23, 2026, with a response deadline of August 7, 2026. The contracting office is located in Silver Spring, Maryland, with performance expected in Frederick, Maryland. Primary point of contact is Shamai Carter, reachable at shamai.m.carter.civ@health.mil, with Nataki Johnson as the secondary contact.

Naval Medical Research Center

POSTED

DEADLINE

Battlefield Pain Management – AnalgesicThis solicitation under the prototype Other Transaction Authority (10 U.S.C. 4022) seeks the development of a single-use analgesic product for acute moderate to severe battlefield pain, with the ultimate goal of obtaining FDA approval. The product must be a combination drug-device system—such as a nasal spray or autoinjector—that is rapid to administer, compact for individual carry, and stable under extreme environmental conditions, capable of withstanding temperature excursions between -25°C and 45°C without refrigeration and maintaining a 2-3 year shelf life at controlled room temperature. It must comply with USP <659> packaging and storage standards, adhere to 21 CFR Part 820 quality system regulations for labeling and control, and meet strict physiological limits including no more than a 20% reduction in baseline blood pressure, heart rate, or blood clotting ability. The product must be classified as a DEA Schedule II or higher controlled substance and must not require special handling for humidity, pressure, or temperature, verified through MIL-STD-810 testing. The effort spans an estimated eight-year period, divided into three sequential objectives: three years for Chemistry, Manufacturing, and Controls (CMC) and stability studies; two years for non-clinical enabling studies; and three years for clinical trials and human factors testing, including potential Emergency Use Authorization (EUA) submission. Deliverables include detailed regulatory documentation, study strategies, interim and final reports, regulatory meeting minutes, protocol approvals from IACUC and ORRC, and full compliance with Controlled Unclassified Information (CUI) marking and data handling protocols. The contract does not fall under FAR or DFARS, but incorporates selected clauses for electronic payment submission, government property management, and termination for convenience. Proposals must be submitted in three volumes—Technical, Management, and Administrative and Cost—with the technical volume limited to 20 pages plus an unlimited attachment for the Statement of Work. A key eligibility requirement is a pass/fail gate: the proposal must demonstrate participation of at least one nontraditional defense contractor or nonprofit research institute, or that all significant participants are small businesses or nontraditional contractors, or that at least one-third of the total project cost is funded by non-federal sources. The proposal deadline has been extended to August 14, 2026, with all submissions required via email in searchable PDF format, compatible with Microsoft Office and Adobe Acrobat, and free of malware, passwords, or hyperlinks.

Defense Health Agency

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DEADLINE

Extended Warranty and Service SupportThe contract entails the provision of ongoing maintenance, technical support, and warranty services for the Leica Stellaris system following its installation, ensuring continued operational reliability and performance. Services are to be delivered in compliance with specified technical standards and response protocols to address system failures, software updates, calibration needs, and user support requests, with an emphasis on minimizing downtime and maximizing system availability. The work is to be performed at the designated place of performance in Bethesda, Maryland, under the oversight of the National Institutes of Health, National Institute of Child Health and Human Development, which operates under the U.S. Department of Health and Human Services. This subcontract is classified under NAICS code 811211, which pertains to medical and dental equipment repair and maintenance, and it was posted on July 22, 2026, with a response deadline of July 31, 2026. The solicitation does not specify a set-aside type or other procurement preferences, and no point of contact information is provided. Bidders must ensure they meet all technical and service requirements for sustaining the Leica Stellaris system in a high-demand research environment, and all deliverables must align with the expectations of the funding agency for uninterrupted scientific operations.

National Institutes Of Health Nichd

POSTED

DEADLINE

Trade-In Equipment Removal and Site CleanupThe contract involves the safe removal, packing, and proper disposal of a decommissioned Leica SP8 microscope located at the National Institutes of Health NICHD facility in Bethesda, Maryland, with a zip code of 20892. This work includes all necessary procedures to dismantle the equipment without risking damage to surrounding infrastructure, secure packaging for transport, and compliant disposal according to environmental and safety regulations. The contractor is also responsible for thorough site cleanup after removal, ensuring the area is left in a condition suitable for the installation of new equipment. All activities must be completed by the response deadline of July 31, 2026, and the work is classified as a subcontract under NAICS code 562998, which covers other environmental cleanup services. The entity responsible for issuance is the Department of Health and Human Services through its NIH NICHD office, though no specific point of contact or set-aside details are provided.

National Institutes Of Health Nichd

POSTED

DEADLINE

Technical Training for End UsersThe contract entails providing hands-on technical training to researchers at the National Institutes of Health, specifically within the NICHD division, on the operation of the Stellaris system. This includes comprehensive instruction on system software, advanced imaging techniques, and routine maintenance procedures to ensure users can effectively and independently utilize the equipment in their research workflows. Training is to be delivered on-site at the NIH campus in Bethesda, Maryland, with a focus on practical, real-world application tailored to the needs of scientific end users. The opportunity is classified as a subcontract under NAICS code 611430, indicating it involves other educational services, and was posted on July 22, 2026, with a response deadline of July 31, 2026, at 3:00 PM. The contracting activity falls under the Department of Health and Human Services, and while no set-aside designation or point of contact details are provided, the place of performance is clearly identified as Bethesda, with a zip code of 20892. All work must be completed at this location, and respondents are expected to demonstrate expertise in delivering technical education for specialized scientific instrumentation.

National Institutes Of Health Nichd

POSTED

DEADLINE

On-Site Installation and Commissioning ServicesThe contract entails the on-site delivery, installation, alignment, calibration, and operational verification of the Leica Stellaris microscope system at the National Institutes of Health in Bethesda, Maryland. The work must be performed in accordance with manufacturer specifications and scientific standards to ensure the system achieves full functionality and meets all performance criteria for research use. All activities, from unboxing and physical placement to final validation, are to be completed at the NIH Bethesda facility by qualified personnel with demonstrated expertise in advanced microscopy systems. The contract is classified as a subcontract under NAICS code 811212, which pertains to office equipment repair and maintenance. It is issued by the National Institute of Child Health and Human Development, a division of the Department of Health and Human Services, with performance required exclusively at the Bethesda location with ZIP code 20892. The solicitation was posted on July 22, 2026, and responses are due by July 31, 2026, by 3:00 p.m. All subcontractor activities must comply with NIH protocols, including safety, documentation, and timeline requirements, and the successful bidder must demonstrate capacity to complete the full commissioning process within the agreed-upon window without disruption to ongoing research operations.

National Institutes Of Health Nichd

POSTED

DEADLINE

Advanced Confocal and 3D-STED Microscope SupplyThe contract seeks the supply of a state-of-the-art Leica Stellaris microscope system equipped with advanced imaging capabilities including confocal, 3D-STED, FLIM, and spectral multiplexing to replace an aging system at the NHLBI Light Microscopy Core. This procurement is intended to enhance the facility’s ability to conduct high-resolution, multi-dimensional biological imaging essential for cutting-edge research. The instrument must meet rigorous technical specifications to support complex experiments requiring precise spatial and temporal resolution, and it must be fully integrated into the existing core infrastructure for seamless operation by trained personnel. The solicitation, classified as a subcontract under NAICS code 334516, is issued by the National Institutes of Health through the Department of Health and Human Services, with performance expected at the Bethesda location with a zip code of 20892. Interested parties must submit responses by the deadline of July 31, 2026, at 3:00 PM EST. The system will serve as a shared resource within the core facility, enabling multi-user access for investigators across multiple research programs focused on cellular and molecular dynamics.

National Institutes Of Health Nichd

POSTED

DEADLINE

Development of Light-Responsive Artificial Cells using Plant-Based Photoreceptor SystemsThe United States Army Corps of Engineers Engineer Research and Development Center Construction Engineering Research Laboratory is seeking to develop light-responsive artificial cells by integrating plant-derived UVR8 photoreceptor systems into synthetic biology platforms, using high-throughput protein engineering and AI-assisted structural refinement to create programmable, pseudo-living systems activated by environmental light stimuli. The project aims to advance foundational science in synthetic biology by leveraging Bioconscientia, LLC’s uniquely specialized expertise in UVR8 photoreceptor technology, which enables precise sensing of UV-B light in a manner unmatched by other entities. Due to the highly specialized nature of the required research and Bioconscientia’s irreplaceable knowledge of existing experimental data and technical pathways, the government intends to award a sole-source contract to this vendor under RFO FAR 12.102(a), with an anticipated award date of September 30, 2026. This presolicitation notice, issued under FAR Part 5.101(a) with solicitation number W9132T26QA015 and NAICS code 541714, does not constitute a formal request for proposals or a competitive procurement, nor is it a set-aside. Interested parties may submit capability statements to CERL-CT-QUOTES@USACE.ARMY.MIL by July 31, 2026, to be reviewed for potential technical equivalency, but submission does not guarantee a change to the government’s acquisition strategy. The government retains full discretion to proceed with sole-source award regardless of responses received. All work will be performed in Champaign, Illinois, and the primary point of contact for submissions is Lurline L. Simmons, with Andrea J. Thomas serving as the contracting officer. No telephone inquiries will be accepted.

W2R2 Construction Engrg Labor

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Leica Microsystems Stellaris Microscope System with Confocal 3D StedThe National Institutes of Health, National Heart, Lung and Blood Institute, is seeking to acquire a single, integrated Stellaris Microscope System with advanced confocal, 3D-STED, fluorescence lifetime imaging (FLIM), and high-plex spectral multiplexing capabilities under a Firm-Fixed-Price Purchase Order. This acquisition is an open market competition with no set-aside, targeting a state-of-the-art laser-scanning platform to replace a 12-year-old Leica SP8 microscope, which will be traded in with removal, packing, and site cleanup included as part of the delivery. The system must support white light laser excitation from 440–790 nm with an acousto-optical beam splitter, prism-based spectral detection spanning 400–850 nm, and at least five Hybrid (HyD) detectors optimized for the full emission range. It must include fully integrated 3D-STED super-resolution with pulsed depletion lasers at 589 nm and 775 nm, time-gated detection for background suppression, and motorized correction collars compatible with oil, glycerin, and water immersion objectives, including a new 86x water-immersion objective chromatically corrected across the full excitation range. FLIM functionality must utilize time-correlated single photon counting with sub-100 picosecond timing resolution and support multi-exponential fitting, lifetime-based unmixing, and integrated enhancement of STED resolution. The platform must enable simultaneous imaging and spectral unmixing of fifteen or more fluorophores using integrated software tools for multiplex panel design. Scanning must allow fast switching between galvo and resonant modes, and the white light laser must include a pulse picker for optimizing FLIM and related applications. All components must operate as a unified, manufacturer-supported system with full software integration. The vendor must deliver, install, and commission the system at the NIH main campus in Bethesda, Maryland, and provide comprehensive user training, a manufacturer warranty, and ongoing service. Quotations must be submitted as a three-volume package: Volume I includes a technical response detailing the system configuration with point-by-point alignment to all salient requirements; Volume II lists up to three relevant past performance contracts; and Volume III provides a complete, itemized price quote inclusive of shipping, installation, training, warranty, and all other associated costs. Any offer of an “equal” product must clearly demonstrate equivalency through detailed technical documentation, including specifications, literature, and a crosswalk

National Institutes Of Health Nichd

POSTED

DEADLINE

AI/ML and Data Analytics for Cardiovascular Device Validation

FDA Office Of Acq Grant Svcs

POSTED

DEADLINE

Chemical, Biological, Radiological, and Nuclear (CBRN) Medical Countermeasure (MCM) Participant Basic Agreement (PBA)The Capability Program Executive for Chemical, Biological, Radiological, and Nuclear Defense (CPE CBRND) is soliciting collaborative participation through a continuous, open Participant Basic Agreement (PBA) under the HEALER portfolio to advance next-generation, threat-agnostic host-directed therapeutics designed to enhance physiological resilience against CBRN threats. This initiative targets five critical biological systems—neurological protection, respiratory stabilization, immune modulation, hematologic and vascular function, and cellular stress and repair pathways—with the goal of developing dual-use medical countermeasures that serve both military and civilian critical care needs. The program invites two categories of collaborators: therapeutic developers with candidates that modulate host response mechanisms and drug development support providers including CROs and CDMOs with capabilities in preclinical testing, clinical trial execution, cGMP manufacturing, regulatory strategy, and advanced modeling. Submission requires a white paper of no more than five pages excluding a cover page, detailing product mechanism of action, efficacy data from validated animal models, regulatory status such as IND experience and clinical trial history, manufacturing capacity and scale-up plans, and company profile for therapeutic developers, or core capabilities and infrastructure for service providers. All participants must express willingness to collaborate with other PBA holders to foster an integrated development ecosystem. The solicitation, issued under statutory authority of 10 U.S.C. §§4021–4023, operates outside the Competition in Contracting Act and does not follow traditional procurement or evaluation frameworks, eliminating standard contract clauses, formal evaluation factors, pricing structures, or submission deadlines. Instead, awards are made at the government’s discretion through a non-traditional acquisition mechanism designed to accelerate innovation. Technical and administrative inquiries are directed to Hunter Robinson and Alexander Mayatte at the U.S. Army’s Aberdeen Proving Ground, Maryland office. Participation prerequisites include current registration in the System for Award Management (SAM), compliance with FDA regulatory pathways, and adherence to cGMP standards for manufacturing. While no specific delivery dates, FOB terms, inspection criteria, or cost estimates are defined, performance is expected to align with the mission of CPE CBRND to enable the Joint Force to operate effectively in CBRN-contested environments. Intellectual property considerations, teaming arrangements, and the scalability of therapeutic candidates are central to selection, with no socioeconomic or size status certifications required. The structure prioritizes agility, collaboration, and cross-sector innovation over rigid compliance, enabling a dynamic pipeline of medical countermeasures capable of addressing evolving biological threats through sustained host resilience.

POSTED

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