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SolicitationsHEALTH AND HUMAN SERVICES, DEPARTMENT OFNAICS 325413

Fisher Scientific Reagents and Consumable Materials for Cell Therapy Manufacturing

HEALTH AND HUMAN SERVICES, DEPARTMENT OF · Solicitation 26-008155 · NAICS 325413 · Unrestricted (full and open) · Closed

Solicitation details

Solicitation number26-008155
Notice ID6300eb88fb754bab906800057e4f1f43
AgencyHEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-tierNATIONAL INSTITUTES OF HEALTH
Contracting officeNATIONAL INSTITUTES OF HEALTH OLAO
NAICS code325413
Product / service code (PSC)6550
Set-asideUnrestricted (full and open)
Notice typePresolicitation
Posted04 August 2026
Response deadline13 August 2026 (closed)
Place of performanceBethesda, MD, USA

Description

NOTICE OF INTENT TO AWARD A SOLE SOURCE CONTRACT Title: Fisher Scientific Reagents and Consumable Materials for Cell Therapy Manufacturing Notice ID (POTS): 26-008155 Product Service Code (PSC): 6550 In Vitro Diagnostic Substances, Reagents, Test Kits, and Sets NAICS Code: 325413 In-Vitro Diagnostic Substance Manufacturing Place of Performance: National Institutes of Health Clinical Center Bethesda, MD 20892 Notice The National Institutes of Health (NIH) Clinical Center intends to award a sole-source firm-fixed-price purchase order to Fisher Scientific for validated reagents and consumable materials required by the Center for Cellular Engineering (CCE) to manufacture FDA-regulated cell-based therapies for use in NIH clinical trials. Requirement The Center for Cellular Engineering (CCE) uses these reagents and consumable materials in the manufacture of FDA-regulated cell-based therapies for patients enrolled in clinical trials at the NIH Clinical Center. All materials have been validated for use in CCE manufacturing processes to ensure they consistently meet the quality standards required to produce safe and effective cell therapy products. Additionally, each material has been reviewed and approved by the CCE Quality Assurance Department, and substitution with alternative products would require extensive revalidation of manufacturing processes, resulting in increased costs, schedule delays, and potential impacts to patient care. Sole-Source Rationale The required reagents and consumables have been validated and approved for use in CCE manufacturing processes. Substituting alternate materials would require extensive requalification, increase costs, delay production, and negatively affect patient care. Fisher Scientific is the only vendor capable of providing the required validated materials and supporting documentation necessary for FDA-regulated manufacturing. Authority The intended sole-source acquisition is authorized under Federal Acquisition Regulation (FAR) 13.106-1(b)(1)(i), which permits solicitation from a single source when the Contracting Officer determines that only one source is reasonably available for an acquisition not exceeding the Simplified Acquisition Threshold. Capability Statements This notice is not a request for quotations or proposals. However, responsible sources that believe they can satisfy the Government's requirement may submit a written capability statement. The Government will evaluate all capability statements received; however, the determination not to compete this requirement remains solely within the Government's discretion. Submission Instructions Capability statements shall reference POTS 26-008155 and must be submitted electronically no later than August 13, 2026, at 6:00 P.M. Eastern Time (ET). Point of Contact Shasheshe Goolsby Team Leader Hospital and Laboratory Support Division Office of Acquisitions and Logistics Management National Institutes of Health Email: shasheshe.goolsby@nih.gov

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Source: this notice on SAM.gov. FedSift republishes public federal procurement data and is not affiliated with the U.S. Government. Always confirm dates and requirements against SAM.gov before responding.