Opportunity

SAM #36C24226Q0604

Radiopharmaceutical Supply for VA Western NY Healthcare System Nuclear Medicine

Buyer

VA Network Contract Office 02

Posted

May 07, 2026

Respond By

May 14, 2026

Identifier

36C24226Q0604

NAICS

424210, 325412

This opportunity involves the procurement of radiopharmaceuticals for the VA Western NY Healthcare System's Nuclear Medicine Department: - Government Buyer: - Department of Veterans Affairs, Western New York Healthcare System (Buffalo) - Products/Services Requested: - Wide range of radiopharmaceuticals, including but not limited to: - Technetium-99m (Tc99m) Sestamibi (various doses) - Tc99m Ceretec, HMPAO WBC, DTPA, DMSA, Hepatolite, Mebrofenin, MAA, MAG3, MDP, Neurolite, Sulfur Colloid, Choletec, Pertechnetate, PYP - Thallium-201 (Tl-201), Iodine-123 (I-123), Iodine-131 (I-131) capsules - Indium-111 (In111) WBC and Octreoscan, Gallium-67 (Ga-67), Gallium-68 (Ga-68) DOTATATE and PSMA - Aerovent Jr kits, Kinevac CCK, Ultra-tag kits, Pyrophosphate kits, sterile water, sealed sources for QC - Emergency delivery services and disposal of depleted sources - Annual quantities specified for each item - Unique/Notable Requirements: - Contractor must be licensed by the US NRC and FDA, and authorized to operate in New York State - Delivery of radiopharmaceuticals within two hours to the Buffalo VA Medical Center - Compliance with all local, state, and federal regulations (NRC, FDA, DOT, DOE) - Provision of quality control documentation, packaging, labeling, and disposal services - Emergency delivery capability and removal/disposal of depleted sealed sources - No specific OEMs or vendors are named; requirement is for licensed radiopharmacy providers

Description

Description This is a combined synopsis/solicitation for commercial products and commercial services prepared in accordance with the format Revolutionary FAR Overhaul (RFO) in Federal Acquisition Regulation (FAR) subpart 12.202, Streamlined Procedures for Evaluation and Solicitation for Commercial Products and Commercial Services, as supplemented with additional information included in this notice. This announcement constitutes the only solicitation; quotes are being requested, and a written solicitation document will not be issued. This solicitation is issued as an RFQ. The solicitation document and incorporated provisions and clauses are those in effect through Federal Acquisition Circular FAC FY26.03A 12/26/2025, FAC 2025-06 10/01/2025. This solicitation is Unrestricted. The associated North American Industrial Classification System (NAICS) code for this procurement is 325412, with a small business size standard of 1300 employees. The FSC/PSC is 6505. The Department of Veterans Affairs Western New York Healthcare System located at 3495 Bailey Avenue, Buffalo, NY 14215 has a requirement for a United States Nuclear Regulatory Commission (US NRC) and Food and Drug Administration (FDA) Licensed Contractor to provide radiopharmaceuticals for the Nuclear Medicine Department for patient care. The VA Western NY Healthcare System at Buffalo intends to award a Base year contract with three Option year firm fixed price contract to a licensed Radiopharmacy authorized to manufacture and distribute Radiopharmaceutical Supplies in New York State with a period of performance of July 1, 2026 through June 30, 2030. The Contractor agrees in accordance with the terms and conditions listed in this statement of work (SOW) to furnish Radiopharmaceuticals in accordance with Local, State, and Federal Regulations. The Contractor shall be able to provide all items listed in the Schedule of Required Supplies with deliveries as needed. Multiple awards shall not be made and subcontracting is not authorized. Under the Atomic Energy Act, the United States Nuclear Regulatory Commission (NRC) is responsible for regulating uses of radioactive material including radio pharmaceuticals. The NRC requires all nuclear medicine facilities to be licensed. The license assures that the facility has a radiation protection program to protect both the patients and the staff. In addition, the staff must meet certain standards of training and experience before they are allowed to administer radioactive material to patients. Each state has one or more radiation programs that ensure safe use of radioactive materials. The NRC has transferred regulatory authority over the use of this material to 34 NRC Agreement States. In these states, the regulatory authority inspects the facility to ensure the staff is trained properly and the equipment is operating safely. The FDA’s Center for Drug Evaluation and Research regulates the radio pharmaceuticals, ensuring effectiveness and patient safety. The mission of the National Institute of Standards and Technology (NIST) is to develop and promote measurement, standards, and technology to enhance productivity, facilitate trade, and improve the quality of life. Although a non-regulatory federal agency, NIST develops the standards for correct patient dosage of radiopharmaceuticals. All interested companies shall provide quotations for the following: Supplies/Services Please Note: Offerors must provide pricing on all items in the Schedule of Required Supplies. Prices quoted are all inclusive including all associated costs including shipping, handling, packaging, storage, licenses etc. excluding emergency delivery, Pharmacist After-Hour Emergency Call-Back, and Weekend White Blood Cell labeling charge. Year 1: July 1, 2026 through June 30, 2027 CLINRadiopharmaceuticalUnit of MeasureQty per yearSizePrice For Each mCi or BulkTotal PriceNumber of Minutes Needed to Prepare Product at RadiopharmacyNDC Of Offered Product 0001Tc99m SestamibiUnit dose1,5008mCi <!-- Additional rows omitted for brevity --> <!-- Additional years and content omitted for brevity --> After hour/Emergency charges VA Western NY Healthcare System at Buffalo Deliveries during normal work hours (Monday - Friday) at no charge. Offeror(s) may list any additional charges below: Deliveries during normal business hours Day No Additional Charges Authorized Emergency Delivery1 Each _______________ Pharmacist After-Hour Emergency Call-Back2 Each ____________ Weekend White Blood Cell labeling charge3 Each ____________ Emergency Delivery: Charge for delivering unscheduled Emergency orders during normal business hours within two (2) hours of receiving the order by phone from the Buffalo VA Medical Center Nuclear Medicine Department. Pharmacist (Emergency after hours): The charge for having a Pharmacist called back to the Pharmacy after hours, prepare the ordered dose and have it delivered to the VA within two hours. (Emergency orders only). Weekend WBC labeling charge: The charge for the Pharmacy to attach a radionuclide to the patient’s white blood cells on a weekend. Base Year Total Price is ________________ Option Year One Total Price is ________________ Option Year Two Total Price is ________________ Option Year Three Total Price is ________________ Total Price for all Four years is ___________________ Statement of Work Radiopharmaceuticals The Contractor shall provide all radiopharmaceuticals identified in the Schedule of Required Supplies to the VA Western NY Healthcare System at Buffalo on a daily and/or as needed basis in accordance with this SOW. Due to the critical need for these supplies in a timely manner, only contractors that are able to complete deliveries within two hours to the VA Western NY Healthcare System at Buffalo need respond to the solicitation. The Contractor shall be licensed by the State of New York. Additionally, the Contractor shall be licensed by the Nuclear Regulatory Commission or another agreement state besides New York and be regularly established in the business of providing radionuclides. The Contractor shall provide copies of these licenses and certifications to the Contracting Officer with their proposal. The Contractor shall provide evidence of being able to make within 2 hours with their proposal. As part of their proposal package, the Contractor shall identify the location of the point of shipment to the address identified under section 1.0 of this SOW. Verification shall be completed utilizing MapQuest, via www.mapquest.com. Deliveries shall incorporate sufficient lead or other high-density metal shielding to comply with all applicable Federal or State standards relating to shipment of radioactive materials. Shipping containers must comply with all Federal and State regulations. This shall include the FDA, DOT, DOE, USNRC, and ICC regulations and standards. Documentation of US DOT package integrity testing shall also be provided. Items must be adequately packaged to prevent damage during handling and storage. All packaging and labeling must meet all Federal and State regulations. All packaging of radioactive material must be clearly labeled radioactive on the outside of the carton in which it is shipped. The Contractor shall label all products delivered to the VA Western NY Healthcare System at Buffalo with the radiopharmaceutical, activity, time of preparation, expiration time, and date. The Contractor shall hold a current unrevoked NRC or an agreement state radioactive materials license, which in addition to other license conditions, would allow for the receipt and disposal of radioactive material and an FDA license to produce and distribute radiopharmaceuticals for human administration. The Contractor shall provide a copy of their radioactive material license with their proposal. The Contractor shall immediately notify the Contracting Officer (CO) and Contracting Officer Representative (COR), upon any action by the NRC or an agreement state and/or FDA to suspend or modify their radioactive materials license. The Contractor shall provide radiopharmaceuticals which have been prepared according to manufacturer’s package inserts and applicable FDA requirements. The Contractor shall perform all quality control procedures as required by Federal and State Regulatory Agencies. The Contractor shall provide with their proposal the below information from letters a through f: The Contractor’s regular work hours. The Contractor’s telephone number for call-in orders during regular work hours. The Contractor’s telephone number and instructions for placing emergency orders after the Contractor’s regular work hours to include weekends. The Contractor’s telephone number for expert advice concerning awarded products. The Contractor shall furnish a statement that any radiopharmaceuticals delivered as “ready-to-use” (individual doses in syringes or vials for single or multiple uses) shall have quality control performed by the Contractor so that the delivered product shall comply with the requirements of the Joint Commission (JC) or with the United States Pharmacopeia. Should any changes occur in the above information during the contract period of performance the Contractor will immediately provide those updated changes in writing to the CO and COR. Current package inserts of all radiopharmaceuticals supplied under the awarded contract shall be shipped to the Nuclear Medicine Service. If any new or updated additions to the package inserts are made available, these shall be sent to the COR at the VA Western NY Healthcare System at Buffalo Nuclear Medicine Service. The Contractor shall make quality control records available to the COR upon written request from the CO or COR. The Contractor shall test all products for quality control periodically. This testing shall be performed at no cost to the Government. The Contractor shall provide a detailed description of the test upon request. The calibration time for each requested radiopharmaceutical is listed in the Schedule of Supplies. If a calibration time is not indicated, then it shall be spelled out in the requirements provided by the Nuclear Medicine Service, otherwise it will correspond to the actual time of delivery. If an ordered dosage of radioactive material is given to the Contractor and it falls within a specified range, then the quantity of radioactivity must be within the dose range provided. If the dose is not given in a range, then the quantity of radioactivity for supplied radiopharmaceuticals must not deviate more than ±20%. Technetium product radiopharmaceuticals not used shall be returned for credit the next work day (including the bulk doses), using the DOT regulations. Credit shall be reflected in the current month’s invoice. The Contractor shall replace any items delivered damaged or in error at no cost to the Government. The COR shall define the replacement date and time. Replacements may be required immediately or within a specified time in accordance with patient care needs. The expiration date and time shall be indicated and affixed to each product as noted below; in general: Ready-to-use doses not shorter than six (6) hours. Tc-99m Pertechnetate not shorter than twelve (12) hours. Kits intended for reconstitution by user not shorter than three (3) months from date of delivery. Unused kits having expiration time not less than two (2) weeks will be exchanged by the Contractor at no additional charge for a comparable kit having the three (3) months life span. If a quality control or material defect is suspected or detected by the COR, the Contractor shall be required to provide any consultation necessary to alleviate any said suspicion or defect by the following: Provide technical expertise in calibration. Provide professional examination of product and submit results and recommendations to the COR. Provide expedient replacement of any product suspected of being deficient. The procedure for labeling of patient’s White Blood Cells (WBC) with Indium-111 Oxine or Tc-Ceretec for re-injecting to the same patient: Telephone requests to the Contractor to arrange for the procedure will take place no later than 3:30 PM for the next workday procedure. Furnishing of the syringe to the Nuclear Medicine Service and pick up of patient’s blood specimen for labeling by the Contractor will be at 7:30 AM or later, if specified by the COR. The return by the Contractor of the patient’s Indium labeled White Blood Cells shall take place not later than within 5 (five) hours from the time of specimen pick up. Pertinent documentation confirming that the identification of the labeled blood specimen matches with the blood specimen of the patient’s blood specimen submitted for labeling procedure. The Contractor shall pick up Radiopharmaceuticals (used and unused) for proper disposal at no cost to the Government. The Contractor shall produce radiopharmaceuticals as described in the Schedule of Supplies. Deliverables and Acceptance Criteria The Contractor shall provide services and staff, and otherwise do all things necessary for or incidental to this Statement of Work, as set forth below: Provide up to two deliveries per day during regular operating hours to the VA Western NY Healthcare System at Buffalo at no additional charge. Delivery charges for STAT orders shall be included on the Schedule of Supplies. STAT deliveries shall average approximately three times a week. Regular daily radiopharmaceutical doses ordered the previous day will be delivered in ONE morning delivery by 7 AM and not split into two separate deliveries with one delivered later in the day. Deliver directly to the Nuclear Medicine Service VA Western NY Healthcare System at Buffalo daily quantity of radiopharmaceuticals by 7:00 AM, as requested from the previous day. In addition to the morning delivery, one more delivery (During Normal Operating Hours) shall be allowed daily at no cost per additional order or emergency. Orders may be placed orally by telephone or fax transmission by ordering officers provided by the Contracting Officer Representative. Deliver directly to the Nuclear Medicine Service VA Western NY Healthcare System at Buffalo quantity of radiopharmaceutical requested on an as needed or emergent basis to arrive in less than two (2) hours after notification. Radioactive dose boxes that are delivered outside of working hours shall be placed in the locked box on floor 4C. The Contractor will have a key to the locked box for this purpose and shall not leave a radioactive materials package at the VA Western NY Healthcare System at Buffalo unless they have verbally communicated this with a Nuclear Medicine staff member. Other delivery times may be outlined by the VA Western NY Healthcare System at Buffalo in this Statement of Work. On federal holidays, no deliveries shall be accepted. Holidays are listed in this SOW. Shipments called when needed may be requested during regular work hours, or after hours as an emergency to include weekends, holidays, and nights. Shipments requested as an emergency shall be delivered as follows: Requests placed after regular work hours (weekends, holidays, and nights) shall be delivered within two (2) hours, or as otherwise specified. Emergency, weekend, and holiday shipments shall be delivered to the location specified by the VA Western NY Healthcare System at Buffalo, unless otherwise specified when called for. All shipments shall be labeled as RADIOACTIVE MATERIAL in compliance with all Federal, State, and Local Laws. All Radiopharmaceuticals, Radioassay Kits, or Analytic Kits shall be furnished by the Contractor in strict accordance with the terms and conditions of the Statement of Work and all applicable Local, State, and Federal Laws. Delivery dates, times, frequency of delivery, specific dosages, and all other specific requirements by the VA Western NY Healthcare System at Buffalo identified within this Statement of Work shall be strictly adhered to. All shipments must have packing slips enclosed providing information about the product and its identification. All invoices shall be submitted electronically through the Tungsten Network and all invoices shall include the purchase order number, product ordered, national drug code, quantity ordered, and the unit price. The Contractor must provide a radiopharmaceutical invoice with each delivery with each dose bar-coded using the Pinestar system. If the Buffalo VA Medical Center’s Pinestar system is not compatible with the bar coding that is provided, then the Contractor must provide whatever software or hardware is necessary to make Buffalo’s system compatible with the Contractor’s barcoding technology. VA OPERATING HOURS The delivery of products provided by the respective awarded contract shall be furnished by the Contractor in accordance with section 3.0 Deliverables and Acceptance Criteria. The Contractor shall not be required except in the case of an emergency to furnish products on a national holiday or during nonworking hours as described below with the exception of normal next day delivery. The following terms have the following meanings: Normal Operating hours of Nuclear Medicine: Monday through Friday, 7:00 AM to 4:30 PM Eastern Standard Time Deliveries shall be accomplished by 7:00 AM and on an as needed basis during normal operating hours. The Contractor shall include up to two (2) deliveries per normal working day during normal working hours as needed at no additional charge. National Holidays: The ten holidays observed by the Federal Government are as follows: New Year's Day, Martin Luther King's Birthday, President's Day, Memorial Day, Independence Day, Labor Day, Columbus Day, Veteran's Day, Thanksgiving, Christmas, and any other day specifically declared by the President of the United States to be a national holiday. CONTRACT AWARD Upon contract award, within five (5) business days, the awarded Contractor shall provide: A copy of their laboratory's current quality control manual to the COR. A dedicated inside sales representative to aid in facilitation in the smooth coordination between the Medical Center and the Contractor's Laboratory Pharmacy. Material safety data sheets and updates on all delivered products as per contract award and any additions throughout the period of performance of the awarded contract. Patient orientation education video presentations and other appropriate material at no additional cost to the Government. The Contractor shall provide signs and posters alerting patients, employees, and the public, of safety precautions in the handling of radioactive materials. QUALITY REQUIREMENTS The Contractor shall guarantee the quality of their radiopharmaceuticals. Quality control shall include pH testing, percent tag, alumina, and 99Mo breakthrough as appropriate. Quality Control shall be performed on each agent dispensed. Complete documentation of quality control results shall be provided upon request. All radiopharmaceuticals shall be calibrated and labeled with concentration, time, total volume, and total activity. Consultation service regarding radiopharmaceutical applications, problems, controls, shall be provided upon request at no charge. On an annual basis, the Contractor shall provide documentation demonstrating compliance with applicable agreement state or NRC license requirements to the Radiation Safety Officer or COR. PERSONNEL POLICY The Contractor is responsible for all costs, including personnel costs, associated with the respective awarded contract unless otherwise specified. Qualifications: Personnel assigned by the Contractor to prepare and provide the products covered within this Statement of Work shall be Nuclear Pharmacists, or a Licensed Technologist working under the supervision of a Nuclear Pharmacist licensed in a State, Territory, or Commonwealth of the United States or the District of Columbia. SPECIAL CONTRACT REQUIREMENTS: HHS/OIG To ensure that the individuals providing services under this respective awarded contract have not engaged in fraud or abuse regarding Sections 1128 and 1128A of the Social Security Act regarding federal health care programs, the Contractor is required to check the Health and Human Services - Office of Inspector General (HHS/OIG), List of Excluded Individuals/Entities on the OIG Website for each person providing services under this contract. The listed parties and entities may not receive Federal Health Care program payments due to fraud and or abuse of the Medicare and Medicaid programs. During the performance of this respective awarded contract the Contractor is prohibited from using any individual or business listed on the List of Excluded Individuals/Entities. Any healthcare provider or entity that employ or enter into contracts with excluded individuals or entities may have a Civil Monetary Penalty imposed against them. By signing their proposal, the Contractor certifies that all persons or entities listed in the Contractor's proposal have been compared against the OIG list and are NOT listed as of the date their proposal was signed. CONTRACTOR STAFF ROLES AND RESPONSIBILITIES The Contractor must be in compliance with all Nuclear Regulatory Commission, United States Pharmacopeia, United States Food and Drug Administration, State, Local, and Joint Commission guidelines, as well as United States Pharmacopeia 797 guidelines. DESIGNATION OF CONTRACT OFFICER REPRESENTATION The Contracting Officer Representative (COR) shall be designated in writing. The COR shall furnish technical guidance and advice regarding the work being performed under the respective awarded contract. The foregoing is not to be construed as authorization to interpret or furnish advice and information to the Contractor relative to the financial or legal aspects of the respective awarded contract. Enforcement of these segments is the sole responsibility of the Contracting Officer. CONTRACTOR RECALL AND SAFETY PLAN AND PROCESS NOTIFICATION TO FACILITY The Contractor shall take immediate action to notify the COR whenever a product, piece of equipment or item is recalled or considered dangerous, hazardous or unsafe in order to remove such products, equipment or items from use. This notification process also applies to safety alerts. The Contractor recall and safety notification plan and process is necessary so that proper notification to individuals who have received or individuals who may utilize such products, equipment, or items can be made in as expedient and efficient manner as possible. The Contractor shall provide to the COR their plan for this safety notification process and also maintain a record system in order to document any safety incident issues by their date, time, and description of the recall or safety alert issue provided to the COR. HIPAA COMPLIANCE The Contractor must adhere to the provisions of Public Law 104-191, Health Insurance Portability and Accountability Act (HIPAA) of 1996 and the National Standards to Protect the Privacy and Security of Protected Health Information (PHI). As required by HIPAA, the Department of Health and Human Services (HHS) has promulgated rules governing the security and use and disclosure of protected health information by covered entities. REQUIRED REGISTRATION WITH CONTRACTOR PERFORMANCE ASSESSMENT SYSTEM (CPARS) As prescribed in Federal Acquisition Regulation (FAR) Part 42.15, the Department of Veterans Affairs evaluates Contractor past performance on all contracts that exceed the thresholds outlined in FAR Part 42.15, and shares those evaluations with other Federal Government Contracting Specialists and Procurement Officials. The FAR requires that the Contractor be provided an opportunity to comment on past performance evaluations prior to the posting of each report. To fulfill this requirement, the Department of Veterans Affairs uses an online database, the Contractor Performance Assessment Reporting System (CPARS). Each Contractor whose contract award is estimated to exceed the thresholds outlined in FAR Part 42.15 is required to provide to the Contracting Officer contact information for the Contractor’s representative with their response to the solicitation. The Contractor is responsible to notify the Contracting Officer of any change to the Contractor’s representative during the contract period of performance. The Contractor’s representative contact information consists of their name, telephone number, and email address. The Government shall register the respective awarded contract within thirty (30) days after contract award. For contracts exceeding one (1) year, the Contracting Officer will evaluate the Contractor’s performance annually. Intermediate reports shall be filed each year until the last year of the contract, when the final report shall be completed. Each report shall be forwarded in CPARS to the Contractor’s designated representative for comment. The Contractor’s representative will have thirty (30) days to submit any comments and return the report to the Contracting Officer. Failure by the Contractor to respond within those thirty (30) days will result in the Government’s evaluation being placed on file in CPARS without any Contractor comments. CONTRACT TERM The respective awarded contract shall be for the Base year with the 3 Option years and the period of performance shall run from July 1, 2026 through June 30, 2030. Schedule of Required Supplies Please Note: Offerors must provide pricing on all items in the Schedule of Required Supplies. Prices quoted are all inclusive including all associated costs including shipping, handling, packaging, storage, licenses etc. excluding emergency delivery, Pharmacist After-Hour Emergency Call-Back, and Weekend White Blood Cell labeling charge. The full text of FAR provisions or clauses may be accessed electronically at https://www.acquisition.gov/browse/index/far. The following solicitation provisions and clause apply to this acquisition: Contract Clauses 52.212-4 Contract terms and conditions-Commercial products and Commercial services. 52.212-5 Contract terms and conditions required to implement statutes or executive orders-Commercial products or Commercial services. 52.217-9 Option to extend the term of the contract (March 2000) 52.222-90 Addressing DEI discrimination by federal contractors. 52.240-91 Security prohibitions and exclusions. 852.204-72 Personnel vetting and credentialing (March2026) 852.211-72 Technical industry standards (Nov2018) 852.232-72 Electronic submission of payment requests. 852.242-71 Administrative Contracting Officer 852.247-73 Packing for domestic shipment 52.252-2 Clauses incorporated by reference 52.212-5 Contract terms and conditions required to implement statutes or executive orders-Commercial products and commercial services (Oct2025) (Deviation Feb2025) Provisions: FAR 52.212-1, Instructions to Offerors Commercial Products and Commercial Services 52.209-7 Information regarding responsibility matters(OCT2018) 52.212-3 Offeror representations and certifications-commercial products and commercials services. 52-216-1 Type of Contract 52.233-2 Service of protest 52.240-90 Security prohibitions and Exclusions Representations and certifications. 52.252-1 Solicitation provisions Incorporated by Reference VAAR 852.233-71 Alternate protest procedure (OCT2018) All quoters shall submit the following: Quotes that itemize and list all requirements according to statement of work and include all items and onsite delivery and installation. All quotes shall be sent to the Contracting Officer - Lorraine.Hussain@va.gov Award will be based upon a comparative evaluation of quotes in accordance with the Simplified Acquisition Procedures of RFO FAR 12. [CO will include basis of evaluation in the quote/offer, e.g., Comparative evaluation is the side by side pairwise comparison of quotes based on factors resulting in a Contracting Officer decision for the quote most favorable to the Government.] FAR 52.212-2 Evaluation-Commercial Products and Commercial Services: In accordance with RFO FAR 12.201-1 and FAR 12.201-2 when appropriate, the contracting officer may (1) Insert the provision at 52.212-2, Evaluation-Commercial Products and Commercial Services, in solicitations for commercial products or commercial services. The following are the decision factors: The quote that meets the combined synopsis requirements and the best value to the government as well as delivery and install timelines. Offerors must complete annual representations and certifications electronically via the System for Award Management (SAM) website located at https://sam.gov/. FAR 52.212-4, Contract Terms and Conditions Commercial Products and Commercial Services. To facilitate the award process, all quotes must include a statement regarding the terms and conditions herein as follows: The terms and conditions in the solicitation are acceptable to be included in the award document without modification, deletion, or addition. Quoters shall list exception(s) and rationale for the exception(s), if any. Submission of your response shall be received not later than 05/14/2026 at 3pm Eastern Standard time emailed to Lorraine.Hussain@va.gov. Late submissions shall be treated in accordance with the solicitation provision at FAR 52.212-1(f). Any questions or concerns regarding this solicitation should be forwarded in writing via e-mail to the Point of Contact listed below. Point of Contact Contracting Officer Lorraine Hussain, Lorraine.Hussain@va.gov Additional Links: Department of Veterans Affairs

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