Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, August 5 at 2:00 PM EDT

Register Free →

Radiation Therapy Quality Management System Deployment and Training

Active
36C25526Q0570Federal

Contract Overview

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

AI Contract Overview

Show more

The VA Medical Center – Overland Park is deploying a comprehensive radiation therapy quality management software system to enhance patient safety by ensuring linear accelerators and related oncology equipment operate within strict tolerances and support routine and patient-specific quality assurance workflows. The contractor is responsible for the full lifecycle of deployment including remote installation, configuration, and verification of the system on the Medical Center’s existing production servers and virtual environment, with coordination for connectivity to treatment machines and the oncology information system. All activities are conducted remotely unless on-site training is required, and the contractor must ensure secure access, proper SSL and firewall configurations, and that all system components function as intended before clinical go-live. The contractor will manage project initiation, develop a communication plan and schedule, validate server readiness, apply machine-specific licenses, and configure interfaces with DICOM-based systems. Machine-specific setup and verification will require about 30 minutes per linear accelerator with physics staff support, followed by integrated testing with the oncology information system. Clinical training will be delivered via six four-hour instructor-led units, either remotely or on-site at the Overland Park facility, with hands-on instruction focused on QA workflows, data review, and reporting. Post-training adoption support will include remote assistance for up to three months per module until clinical acceptance is achieved, culminating in a signed Project Acceptance Form. The entire effort is expected to conclude within four months of project kick-off, with all education and deployment services expiring one year from that date. The VA provides all necessary hardware, network access, documentation, and security credentials, while the contractor assumes responsibility for software installation, configuration, and training delivery under strict VA security protocols and change management procedures.

General Info

Deploy radiation therapy software remotely with full configuration, training, and support within four months under VA security protocols.

Agency

Department Of Veterans Affairs → 255-NETWORK Contract Office 15 (36C255)View Agency

NAICS

332510 - Hardware ManufacturingView NAICS

Place of Performance

Kansas City, MO, 64128, USA

Set-Aside

NONE

Documents

(1)

36C25526Q0570.pdf

PDF

AI Contract Breakdown

Uniform Contract Format

What is UCF?

Uniform Contract Format (UCF) uses AI to break down any contract into standardized sections—scope, pricing, deliverables, and evaluation criteria.

Timeline

PhaseSources Sought
Posted

Sources Sought

Response Deadline

Submission deadline

Response Deadline

Ready to pursue this opportunity?

Start your free trial to track this contract, build proposals with AI assistance, and manage your pipeline.

Organization & Contact Information

Show more
AgencyDepartment Of Veterans Affairs → 255-NETWORK Contract Office 15 (36C255)
Contacts1 person available
OfficeLEAVENWORTH, KS, 66048, USA
Organization / Agency
Department Of Veterans Affairs → 255-NETWORK Contract Office 15 (36C255)
View Agency Profile
Office AddressLEAVENWORTH, KS, 66048, USA

Full Description

Show more

STATEMENT OF WORK



SOW as of: 6/3/2026



2. Contract Title


Radiation Therapy Quality Management System Deployment and Training.


3. Background


The VA Medical Center – Overland Park requires a comprehensive software system to support quality assurance for radiotherapy treatment delivery and associated treatment machines. This effort will enable the facility to improve patient safety by verifying that radiotherapy treatment machines operate within defined tolerances and by supporting routine and patient‑specific quality assurance workflows.


The work described in this SOW covers the initial deployment, configuration, and clinical adoption support for a new quality management software system for linear accelerators and related oncology information systems. It includes remote installation, configuration, verification, training, and adoption support necessary to achieve clinical “go‑live” at the VA Medical Center – Overland Park.


4. Scope


The scope of this SOW includes all contractor activities necessary to deploy the radiation therapy quality management software system in the VA Medical Center – Overland Park production environment, configure it for use with existing treatment machines and oncology information systems, verify correct operation, train clinical and technical staff, and support adoption through initial clinical use.


The work will be performed primarily via remote services, with coordination among Medical Center project leadership, information technology staff, and clinical staff. The scope is limited to the Medical Center’s production data center and associated radiotherapy equipment and does not extend to other facilities or systems beyond those explicitly identified herein.


5. Specific Tasks


5.1 Task 1 – Project Management and Initiation


The contractor shall provide project management services to plan, coordinate, and oversee all deployment activities. This includes identification of key project personnel (Executive Sponsor, Project Manager, IT Lead, and Clinical Lead), development of a communication plan, and coordination of all dependencies required to initiate the project.


Subtask 5.1.1 – Project Initiation


  • Confirm and review all aspects of the order and associated deliverables.
  • Discuss preliminary dependencies such as server readiness, virtual environment requirements, linear accelerator prerequisites, and any required beam modeling activities.
  • Identify project goals, objectives, and additional stakeholders.
  • Establish the communication plan (methods, types, style, and schedule of status updates and meetings).

Deliverables (Task 1):


  • Project communication plan.
  • Initial project schedule and milestone list.

5.2 Task 2 – System Installation and Environment Configuration


The contractor shall perform remote installation of the quality management software system to the latest approved version on the Medical Center’s designated production server(s) in a new virtual environment.


Subtask 5.2.1 – Pre‑Installation Validation


  • Validate that the production server(s) meet required CPU, RAM, storage, and graphics specifications.
  • Verify network attachment, connectivity, and performance levels necessary to support expected user experience.
  • Confirm availability of necessary software licenses for installation.

Subtask 5.2.2 – Software Installation


  • Install the quality management software application and associated server components on the identified production server(s).
  • Configure server and database components in accordance with vendor specifications.
  • Apply the purchased machine‑specific license(s) associated with this deployment.

Subtask 5.2.3 – Security and Connectivity Configuration


  • Assist with configuration of required secure socket layer (SSL) capabilities on the quality management servers, using an SSL certificate provided by the VA Medical Center – Overland Park, if applicable.
  • Assist with Windows firewall configuration on the quality management server(s) or associated hardware as required for proper operation.

Deliverables (Task 2):


  • Installed and configured production software environment.
  • Installation validation checklist documenting server readiness and software installation completion.

5.3 Task 3 – Machine Configuration and Verification


Following installation, the contractor shall configure the software system for the Medical Center’s treatment machines (linear accelerators) and perform verification testing.


Subtask 5.3.1 – Machine Configuration


  • Use machine‑specific information provided by the Medical Center to configure each treatment machine within the system.
  • Establish connectivity with devices and imaging/QA equipment as applicable.

Subtask 5.3.2 – Machine Verification


  • For each machine, perform verification testing of connectivity and data transfer, requiring approximately 30 minutes per machine with physics support from Medical Center staff.
  • Confirm that the system is technically functioning and receiving data from each machine as expected.

Deliverables (Task 3):


  • Completed machine configuration for each designated treatment machine.
  • Machine verification record for each configured machine.
  • Technical sign‑off form submitted to Medical Center key stakeholder for signature.

5.4 Task 4 – Interface with Oncology Information System (OIS)


The contractor shall assist with establishing remote connection between the quality management system and the existing oncology information system instance used by the VA Medical Center – Overland Park.


Subtask 5.4.1 – OIS Connectivity


  • Collaborate with Medical Center staff and the OIS vendor, as required, to configure and test storage and query/retrieve of studies between systems.
  • Confirm that a single OIS instance is configured to communicate with the quality management system.

Deliverables (Task 4):


  • Documented interface configuration parameters.
  • OIS connectivity test results.

5.5 Task 5 – Clinical Application Education


The contractor shall provide remote and/or on‑site education services to support clinical use of the quality management system. The Medical Center has purchased six education units, where one unit equals a four‑hour remote instructor‑led session, with a minimum of two days (six units) required to schedule an on‑site event.


Subtask 5.5.1 – Education Planning and Preparation


  • Conduct a remote training preparation session to ensure required files, calibrations, and readiness tasks are complete prior to formal training.
  • Develop and share training agendas with Medical Center staff.

Subtask 5.5.2 – Product Training


  • Deliver remote and/or on‑site training tailored to the Medical Center’s workflows, focusing on routine imaging QA, machine QA, and patient‑related QA modules as applicable.
  • Provide hands‑on instruction for clinical users, focusing on system navigation, data review, reporting, and decision‑making workflows.

Deliverables (Task 5):


  • Training agendas and schedule.
  • Completion record of training sessions, including participant lists and topics covered.

5.6 Task 6 – Adoption Support and Clinical Go‑Live


The contractor shall support the Medical Center’s adoption of the system through a defined post‑training period, culminating in clinical go‑live.


Subtask 5.6.1 – Adoption Planning


  • Collaborate with the Medical Center clinical lead to define an adoption plan for each system module deployed, including timelines and acceptance criteria.

Subtask 5.6.2 – Remote Adoption Support


  • Provide a designated resource to offer remote support for a defined period (typically one to three months per module, or until go‑live, whichever is sooner).
  • Assist with clinical acceptance testing, including agreed‑upon test cases and evaluation of system outputs.

Subtask 5.6.3 – Project Completion and Transition


  • Facilitate final project status meeting to confirm that all deliverables and milestones have been met.
  • Support completion of the Project Acceptance Form by the Medical Center.
  • Transition ongoing support responsibilities to the vendor’s global support organization or equivalent.

Deliverables (Task 6):


  • Adoption plan and acceptance testing documentation.
  • Final project status report.
  • Signed Project Acceptance Form.

6. Performance Monitoring


The COR will monitor contractor performance through review of deliverables, participation in status meetings, and verification that milestones (installation complete, verification complete, training complete, client testing complete, and clinical go‑live) are achieved in accordance with the agreed project schedule.


Contractor performance will be considered acceptable when all tasks are completed, the system is operational in the production environment, necessary interfaces and machine configurations are verified, staff training is complete, and the Medical Center has documented acceptance of clinical use.


7. Security, Privacy, and Access Requirements


Contractor personnel will require remote access to designated servers to perform installation, configuration, and support activities; such access shall be provided in accordance with VA and facility policies. Service accounts created for the system (for example, administrative and database service accounts) must be configured to avoid password expiration or unmanaged changes that would disrupt system operation; changes that impact connectivity may require additional remote support sessions.


The Medical Center will ensure that applicable VA security, privacy, and information protection requirements are followed, including completion of any required VA forms and background checks, as directed by the Information Security Officer (ISO).


8. Government‑Furnished Equipment (GFE) / Government‑Furnished Information (GFI)


The VA Medical Center – Overland Park will provide:


  • Production server(s) and virtual environment meeting required specifications, connected to the facility LAN/WAN.
  • Access to DICOM source systems, IP network, and security infrastructure necessary for installation and configuration.
  • Relevant configuration documentation (e.g., automation configuration spreadsheet, network configuration details, and machine configuration data).

No contractor‑furnished hardware is included in this SOW.


9. Other Pertinent Information or Special Considerations


  • All contractor project management, installation, configuration, verification, training, and adoption assistance activities will be performed remotely unless otherwise specified in this document.
  • The Medical Center will coordinate directly with linear accelerator vendors to install and configure any third‑party licenses and software required for automation (e.g., imaging systems or file synchronization tools).
  • The Medical Center is responsible for obtaining and providing any required SQL licenses, CALs, or SSL certificates.

10. Place of Performance


Place of performance is primarily remote, with work performed via secure remote access to the VA Medical Center – Overland Park systems. When on‑site services are scheduled (e.g., on‑site training), work will occur at:


VA Medical Center – Overland Park
10500 Mastin Rd
Overland Park, KS 66212


11. Period of Performance


The period of performance will commence upon issuance of the purchase order and project kick‑off. Deployment activities, including installation, configuration, verification, training, and adoption support, are expected to be completed within approximately four months from project kick‑off, with final duration dependent on project complexity and resource availability. Education and deployment services expire one year from project kick‑off date.


12. Delivery Schedule (Key Milestones)


SOW Task


Deliverable / Milestone


Due Date (Calendar Days After CO Start)


5.1


Project communication plan and schedule


Within 14 days of order completion 


5.2


Installation complete


Within 6 weeks after accurate data confirmed 


5.3–5.4


Machine and OIS configuration and verification


Within 4 weeks of project kick‑off 


5.5


Training complete


Within 2 weeks after verification 


5.6


Client testing complete and clinical go‑live


Duration dependent on module complexity, generally ≤ 90 days 


5.6


Final status report and Project Acceptance Form


Upon successful clinical go‑live 


Specific dates will be finalized in the project schedule at initiation.


13. Change Management


Any change to the scope, requirements, technical components, schedule, or costs described in this SOW shall require a formal, written change request. The change request shall describe the requested change, identify required actions to execute the change, estimate impacts to schedule and cost, and include signatures/approvals from both parties before implementation.



STATEMENT OF WORK



SOW as of: 6/3/2026



2. Contract Title


Radiation Therapy Quality Management System Deployment and Training.


3. Background


The VA Medical Center – Overland Park requires a comprehensive software system to support quality assurance for radiotherapy treatment delivery and associated treatment machines. This effort will enable the facility to improve patient safety by verifying that radiotherapy treatment machines operate within defined tolerances and by supporting routine and patient‑specific quality assurance workflows.


The work described in this SOW covers the initial deployment, configuration, and clinical adoption support for a new quality management software system for linear accelerators and related oncology information systems. It includes remote installation, configuration, verification, training, and adoption support necessary to achieve clinical “go‑live” at the VA Medical Center – Overland Park.


4. Scope


The scope of this SOW includes all contractor activities necessary to deploy the radiation therapy quality management software system in the VA Medical Center – Overland Park production environment, configure it for use with existing treatment machines and oncology information systems, verify correct operation, train clinical and technical staff, and support adoption through initial clinical use.


The work will be performed primarily via remote services, with coordination among Medical Center project leadership, information technology staff, and clinical staff. The scope is limited to the Medical Center’s production data center and associated radiotherapy equipment and does not extend to other facilities or systems beyond those explicitly identified herein.


5. Specific Tasks


5.1 Task 1 – Project Management and Initiation


The contractor shall provide project management services to plan, coordinate, and oversee all deployment activities. This includes identification of key project personnel (Executive Sponsor, Project Manager, IT Lead, and Clinical Lead), development of a communication plan, and coordination of all dependencies required to initiate the project.


Subtask 5.1.1 – Project Initiation


  • Confirm and review all aspects of the order and associated deliverables.
  • Discuss preliminary dependencies such as server readiness, virtual environment requirements, linear accelerator prerequisites, and any required beam modeling activities.
  • Identify project goals, objectives, and additional stakeholders.
  • Establish the communication plan (methods, types, style, and schedule of status updates and meetings).

Deliverables (Task 1):


  • Project communication plan.
  • Initial project schedule and milestone list.

5.2 Task 2 – System Installation and Environment Configuration


The contractor shall perform remote installation of the quality management software system to the latest approved version on the Medical Center’s designated production server(s) in a new virtual environment.


Subtask 5.2.1 – Pre‑Installation Validation


  • Validate that the production server(s) meet required CPU, RAM, storage, and graphics specifications.
  • Verify network attachment, connectivity, and performance levels necessary to support expected user experience.
  • Confirm availability of necessary software licenses for installation.

Subtask 5.2.2 – Software Installation


  • Install the quality management software application and associated server components on the identified production server(s).
  • Configure server and database components in accordance with vendor specifications.
  • Apply the purchased machine‑specific license(s) associated with this deployment.

Subtask 5.2.3 – Security and Connectivity Configuration


  • Assist with configuration of required secure socket layer (SSL) capabilities on the quality management servers, using an SSL certificate provided by the VA Medical Center – Overland Park, if applicable.
  • Assist with Windows firewall configuration on the quality management server(s) or associated hardware as required for proper operation.

Deliverables (Task 2):


  • Installed and configured production software environment.
  • Installation validation checklist documenting server readiness and software installation completion.

5.3 Task 3 – Machine Configuration and Verification


Following installation, the contractor shall configure the software system for the Medical Center’s treatment machines (linear accelerators) and perform verification testing.


Subtask 5.3.1 – Machine Configuration


  • Use machine‑specific information provided by the Medical Center to configure each treatment machine within the system.
  • Establish connectivity with devices and imaging/QA equipment as applicable.

Subtask 5.3.2 – Machine Verification


  • For each machine, perform verification testing of connectivity and data transfer, requiring approximately 30 minutes per machine with physics support from Medical Center staff.
  • Confirm that the system is technically functioning and receiving data from each machine as expected.

Deliverables (Task 3):


  • Completed machine configuration for each designated treatment machine.
  • Machine verification record for each configured machine.
  • Technical sign‑off form submitted to Medical Center key stakeholder for signature.

5.4 Task 4 – Interface with Oncology Information System (OIS)


The contractor shall assist with establishing remote connection between the quality management system and the existing oncology information system instance used by the VA Medical Center – Overland Park.


Subtask 5.4.1 – OIS Connectivity


  • Collaborate with Medical Center staff and the OIS vendor, as required, to configure and test storage and query/retrieve of studies between systems.
  • Confirm that a single OIS instance is configured to communicate with the quality management system.

Deliverables (Task 4):


  • Documented interface configuration parameters.
  • OIS connectivity test results.

5.5 Task 5 – Clinical Application Education


The contractor shall provide remote and/or on‑site education services to support clinical use of the quality management system. The Medical Center has purchased six education units, where one unit equals a four‑hour remote instructor‑led session, with a minimum of two days (six units) required to schedule an on‑site event.


Subtask 5.5.1 – Education Planning and Preparation


  • Conduct a remote training preparation session to ensure required files, calibrations, and readiness tasks are complete prior to formal training.
  • Develop and share training agendas with Medical Center staff.

Subtask 5.5.2 – Product Training


  • Deliver remote and/or on‑site training tailored to the Medical Center’s workflows, focusing on routine imaging QA, machine QA, and patient‑related QA modules as applicable.
  • Provide hands‑on instruction for clinical users, focusing on system navigation, data review, reporting, and decision‑making workflows.

Deliverables (Task 5):


  • Training agendas and schedule.
  • Completion record of training sessions, including participant lists and topics covered.

5.6 Task 6 – Adoption Support and Clinical Go‑Live


The contractor shall support the Medical Center’s adoption of the system through a defined post‑training period, culminating in clinical go‑live.


Subtask 5.6.1 – Adoption Planning


  • Collaborate with the Medical Center clinical lead to define an adoption plan for each system module deployed, including timelines and acceptance criteria.

Subtask 5.6.2 – Remote Adoption Support


  • Provide a designated resource to offer remote support for a defined period (typically one to three months per module, or until go‑live, whichever is sooner).
  • Assist with clinical acceptance testing, including agreed‑upon test cases and evaluation of system outputs.

Subtask 5.6.3 – Project Completion and Transition


  • Facilitate final project status meeting to confirm that all deliverables and milestones have been met.
  • Support completion of the Project Acceptance Form by the Medical Center.
  • Transition ongoing support responsibilities to the vendor’s global support organization or equivalent.

Deliverables (Task 6):


  • Adoption plan and acceptance testing documentation.
  • Final project status report.
  • Signed Project Acceptance Form.

6. Performance Monitoring


The COR will monitor contractor performance through review of deliverables, participation in status meetings, and verification that milestones (installation complete, verification complete, training complete, client testing complete, and clinical go‑live) are achieved in accordance with the agreed project schedule.


Contractor performance will be considered acceptable when all tasks are completed, the system is operational in the production environment, necessary interfaces and machine configurations are verified, staff training is complete, and the Medical Center has documented acceptance of clinical use.


7. Security, Privacy, and Access Requirements


Contractor personnel will require remote access to designated servers to perform installation, configuration, and support activities; such access shall be provided in accordance with VA and facility policies. Service accounts created for the system (for example, administrative and database service accounts) must be configured to avoid password expiration or unmanaged changes that would disrupt system operation; changes that impact connectivity may require additional remote support sessions.


The Medical Center will ensure that applicable VA security, privacy, and information protection requirements are followed, including completion of any required VA forms and background checks, as directed by the Information Security Officer (ISO).


8. Government‑Furnished Equipment (GFE) / Government‑Furnished Information (GFI)


The VA Medical Center – Overland Park will provide:


  • Production server(s) and virtual environment meeting required specifications, connected to the facility LAN/WAN.
  • Access to DICOM source systems, IP network, and security infrastructure necessary for installation and configuration.
  • Relevant configuration documentation (e.g., automation configuration spreadsheet, network configuration details, and machine configuration data).

No contractor‑furnished hardware is included in this SOW.


9. Other Pertinent Information or Special Considerations


  • All contractor project management, installation, configuration, verification, training, and adoption assistance activities will be performed remotely unless otherwise specified in this document.
  • The Medical Center will coordinate directly with linear accelerator vendors to install and configure any third‑party licenses and software required for automation (e.g., imaging systems or file synchronization tools).
  • The Medical Center is responsible for obtaining and providing any required SQL licenses, CALs, or SSL certificates.

10. Place of Performance


Place of performance is primarily remote, with work performed via secure remote access to the VA Medical Center – Overland Park systems. When on‑site services are scheduled (e.g., on‑site training), work will occur at:


VA Medical Center – Overland Park
10500 Mastin Rd
Overland Park, KS 66212


11. Period of Performance


The period of performance will commence upon issuance of the purchase order and project kick‑off. Deployment activities, including installation, configuration, verification, training, and adoption support, are expected to be completed within approximately four months from project kick‑off, with final duration dependent on project complexity and resource availability. Education and deployment services expire one year from project kick‑off date.


12. Delivery Schedule (Key Milestones)


SOW Task


Deliverable / Milestone


Due Date (Calendar Days After CO Start)


5.1


Project communication plan and schedule


Within 14 days of order completion 


5.2


Installation complete


Within 6 weeks after accurate data confirmed 


5.3–5.4


Machine and OIS configuration and verification


Within 4 weeks of project kick‑off 


5.5


Training complete


Within 2 weeks after verification 


5.6


Client testing complete and clinical go‑live


Duration dependent on module complexity, generally ≤ 90 days 


5.6


Final status report and Project Acceptance Form


Upon successful clinical go‑live 


Specific dates will be finalized in the project schedule at initiation.


13. Change Management


Any change to the scope, requirements, technical components, schedule, or costs described in this SOW shall require a formal, written change request. The change request shall describe the requested change, identify required actions to execute the change, estimate impacts to schedule and cost, and include signatures/approvals from both parties before implementation.



Similar Contracts

Same NAICS industry code

NAICS: 332510
New
DIBBS
INSERT, SCREW THREAD
Solicitation # SPE4A6-26-T-11KR
The contract pertains to the procurement of 19 screw thread inserts with NSN 5325-01-125-3163, issued under solicitation SPE4A6-26-T-11KR by the ASC Commodities Division of the Department of Defense. The delivery is scheduled for 567 days after award, and the solicitation was posted on August 3, 2026, with responses due by August 11, 2026. The item is subject to strict export control regulations under either ITAR or EAR, meaning any disclosure of associated technical data to foreign persons—including foreign nationals within the United States—is prohibited without prior authorization from the Department of State or Department of Commerce. DFARS 252.225-7048 governs the handling of this controlled information. Access to the export-controlled technical data is restricted to DLA contractors who hold a valid US/Canada Joint Certification Program certification, have completed mandatory training on proper handling of DOD export-controlled technical data, and have successfully submitted and been approved for the DLA Export-Controlled Technical Data Questionnaire. Distribution is tightly controlled to ensure compliance with U.S. national security policies, and all recipients must be formally authorized by the DLA controlling authority. The place of performance is identified as New Cumberland, Pennsylvania, with Duane Watkins Jr. designated as the primary point of contact for inquiries.
ASC COMMODITIES DIVISION

POSTED

about 9 hours ago

DEADLINE

in 8 days
View Details
NAICS: 332510
New
DIBBS
COVER, ACCESS
Solicitation # SPE4A6-26-Q-1254
The contract pertains to the procurement of 49 units of COVER, ACCESS with NSN 5340-00-870-1655 under solicitation SPE4A6-26-Q-1254, with a delivery deadline of 358 days after date of order. All items must be produced and delivered from origin with inspection and acceptance occurring at origin, and are subject to strict packaging requirements outlined in DLA’s RP001 and MIL-STD-129, including commercial packaging per ASTM D3951 unless hazardous material is involved, in which case FED-STD-313 and TQ requirement IP025 apply. Item unique identification is waived per the service customer’s request, and DFARS 252.211-7003(c)(1)(i) governs marking and labeling. Sampling must follow MIL-STD-1916 or ASQ H1331 Table 1 using zero-defect acceptance criteria unless otherwise specified, with critical, major, and minor attributes assigned verification levels VII, IV, and II or AQLs of 0.1, 1.0, and 4.0 respectively. The supplier must comply with a suite of technical and quality requirements including RQ001 for tailored higher-level quality standards, RQ042 for ISO 9001:2015, RT001 for measurement and test equipment calibration, and RD004 for CMMC Level 2 self-assessment certification. Configuration changes require formal engineering change proposal requests under RQ002, and government identification must be removed from non-accepted supplies as per RQ011. All requirements referenced by R or I numbers derive from the DLA Master List of Technical and Quality Requirements, with revision control tied to the solicitation or award date depending on acquisition size. Deliveries must be palletized per RP001 and shipped to the designated DLA Distribution Depot in Tinker AFB, Oklahoma, with transportation governed by DLAD Proc Note C19 and C20. The contract enforces a strict 0% quantity variance and is classified as a Critical Application Item for The Boeing Company.
ASC COMMODITIES DIVISION

POSTED

about 9 hours ago

DEADLINE

in 9 days
View Details
NAICS: 332510
New
DIBBS
STRAP, WEBBING
Solicitation # SPE7LX-26-U-9155
This contract specifies the procurement of STRAP, WEBBING under solicitation SPE7LX-26-U-9155, with a total quantity of 5,051 units at a unit price of $5,051.00, delivered FOB origin within 67 days. The item is identified by NSN 5340-01-659-7728 and part number HS404H, and must conform to source-controlled drawings and technical requirements referenced in the DLA Master List of Technical and Quality Requirements, which override all other standards including ASTM D3951. Packing and labeling must comply with MIL-STD-129 and DLA Packaging Requirements, with hazardous material handled per FED-STD-313 and TQ requirement IP025, otherwise commercially packaged per ASTM D3951. The contract prohibits use of Class I ozone-depleting chemicals and requires approval for any substitute chemicals. Configuration changes must follow an Engineering Change Proposal process, and deviations require formal variance requests. Certificate of Conformance procedures are authorized unless suspended by a Quality Assurance Letter of Instruction. Only approved sources listed on the source-controlled drawing may supply the item, though additional qualified sources may be recognized without drawing revision. The procurement is a total small business set-aside under NAICS 332510, with inspection and acceptance conducted at destination and no variance allowed in quantity. All packaging must be palletized in accordance with DLA requirements, and the unit of issue is EA per contract specifications.
STRATEGIC ACQ PROGRAM DIRECTORATE

POSTED

about 9 hours ago

DEADLINE

in 15 days
View Details
NAICS: 332510
New
DIBBS
SHEET, METAL
Solicitation # SPE7M0-26-T-026L
The contract pertains to the procurement of 20 units of sheet metal identified by NSN 9535-01-348-3224 under solicitation SPE7M0-26-T-026L, with a delivery requirement of five days after order date. All items must comply with technical and quality standards referenced in the DLA Master List of Technical and Quality Requirements, with the applicable revision determined by the solicitation or award date depending on the acquisition size. Packaging must adhere to DLA specifications, and all government identification must be removed from non-accepted supplies. The material must be free of asbestos, and any substitutes require formal approval under clause L30 and provision 4 conditions. Mercury and mercury-containing compounds are prohibited from intentional addition or direct contact with the supplied hardware, except for functional uses in batteries, fluorescent lights, specified instruments, sensors, controls, weapon systems, and chemical analysis reagents approved by NAVSEA. Portable fluorescent lamps and instruments containing mercury must be shockproof and feature a secondary containment barrier in accordance with NAVSEA 5100-003D. Identification markings must conform to MIL-STD-130N dated November 16, 2012. The contract is issued by the Department of Defense through the Maritime Supply Chain ESOC Buys office with performance occurring at Pearl Harbor, Hawaii. The primary point of contact is Grace Beck, reachable via email and phone provided. The solicitation was posted on August 3, 2026, with responses due by August 14, 2026, under a federal acquisition framework governed by NAICS code 332510.
MARITIME SUPPLY CHAIN ESOC BUYS

POSTED

about 9 hours ago

DEADLINE

in 11 days
View Details
NAICS: 332510
New
DIBBS
RING, RETAINING
Solicitation # SPE4A6-26-T-11LC
The contract specifies the procurement of 60 retaining rings with NSN 5325-01-602-6198 under solicitation SPE4A6-26-T-11LC, requiring delivery within 227 days to the DLA Distribution facility in New Cumberland, Pennsylvania. All items must comply with DLA packaging requirements per MIL-STD-2073-1E and marking standards per MIL-STD-129, with no special marking required. Packaging must use preservation method 10, dry, with no cushioning or dunnage, in bulk outer packaging, and palletization must adhere to DLA’s specified guidelines. Mercury and mercury-containing compounds are strictly prohibited in the product, preservation, packaging, packing, and marking materials, except for limited functional uses in batteries, lamps, instruments, sensors, controls, weapon systems, or chemical reagents specified by NAVSEA, with portable mercury-containing devices requiring shock-proof design and a secondary containment barrier. The unit price is $60.00 per EA, totaling $3,600, with zero variance allowed in quantity. Inspection and acceptance occur at destination, and delivery is FOB origin. All technical and quality requirements referenced by R or I numbers are governed by the DLA Master List, with the applicable revision determined by the solicitation or award date. The contract is issued under DoD unit of issue, with freight and shipping addresses confirmed for the New Cumberland facility, and transportation governed by DLA procedural notes C19 and C20.
ASC COMMODITIES DIVISION

POSTED

about 9 hours ago

DEADLINE

in 8 days
View Details
NAICS: 332510
New
DIBBS
RING, EXTERNALLY THREAD
Solicitation # SPE4A5-26-T-319R
The contract specifies the procurement of two externally threaded rings with NSN 5365-01-005-1901 and part number 41002372 from WOODWARD HRT INC, to be delivered within 20 days to the Taiwan Army’s Zuo-Ying Ammunition Sub facility in Kaohsiung City. Delivery is FOB origin with no variance allowed in quantity, and inspection and acceptance occur at the origin point. Packaging must comply with MIL-STD-2073-1E, including specific preservation methods, wrapping, and container standards, while marking adheres strictly to MIL-STD-129 with no special markings required. Palletization follows DLA packaging requirements, and unit of issue is each. Sampling and quality verification follow MIL-STD-1916 or comparable zero-based plans, with critical, major, and minor attributes assigned verification levels VII, IV, and II or AQLs of 0.1, 1.0, and 4.0 respectively; unspecified attributes are treated as major. Item Unique Identification is not required per DFARS 252.211-7003(c)(1)(i). Technical and quality requirements are governed by the DLA Master List referenced in RQ017 and RA001, with revision control dependent on solicitation or award date. The contract is issued under SPE4A5-26-T-319R, with a response deadline of August 11, 2026, and is classified under NAICS code 332510. Funds are allocated for delivery by August 4, 2026, and government-use data includes procurement codes and logistics designators.
ASC SUPPLIER OPER OEM DIVISION

POSTED

about 9 hours ago

DEADLINE

in 8 days
View Details
NAICS: 332510
New
DIBBS
TIE DOWN, CARGO, VEHI
Solicitation # SPE7L1-26-T-907P
This contract pertains to the procurement of 18 units of a tie-down cargo system for vehicles, identified by NSN 5340-01-730-7892 and part number R2616SH-B from RATCHET DEPOT INC. The delivery is required within 176 days from the contract date, with shipment originating FOB origin and no variance allowed in quantity. Inspection and acceptance occur at the destination facility. All items must comply strictly with DLA’s Master List of Technical and Quality Requirements, which supersede other standards including ASTM D3951, and packaging must adhere to MIL-STD-129 and RP001 for DLA packaging guidelines. The use of Class I ozone-depleting chemicals is categorically prohibited, and any substitutes must be pre-approved unless explicitly permitted by the specification. Items must be marked in accordance with MIL-STD-130N for identification of U.S. military property. Hazardous materials, if applicable, must be packaged per TQ requirement IP025 as defined in FED-STD-313, otherwise commercial packaging per ASTM D3951 is acceptable, provided DLA Master List requirements override it. Palletization must meet DLA’s packaging standards. The delivery destination is the DLA Distribution facility at New Cumberland, Pennsylvania, and the unit of issue is each, with no allowance for partial shipments. The contract was solicited under SPE7L1-26-T-907P with a response deadline of August 14, 2026, and the required ship date is February 7, 2027. The responsible point of contact is Rodney McNinch of the Department of Defense’s Land Supply Chain.
LAND SUPPLY CHAIN

POSTED

about 9 hours ago

DEADLINE

in 11 days
View Details

More opportunities from Department Of Veterans Affairs → 255-NETWORK Contract Office 15 (36C255)

Same awarding agency

NAICS: 611430
New
Federal
U099 - Competency Annual Nurse Training - KCVA
Solicitation # 36C25526Q0567
The Kansas City VA Medical Center is seeking information from potential vendors to provide annual competency training services licensed through Elsevier for nursing staff, covering essential modules such as ECG rhythm recognition, emergency nursing orientation, mental and behavioral health, home health collection, ambulatory skills, pharmacology, and nursing professional development. The requirement is structured as a Base Year with four optional extension years, and all training must be delivered exclusively via Elsevier’s platform. Vendors must submit written proof of formal authorization or licensure from Elsevier to offer these services; responses lacking this documentation will not be considered. No quotes are being solicited at this time, and the effort is strictly for market research to gauge vendor availability and capability. The solicitation, identified as U099 - Competency Annual Nurse Training - KCVA under solicitation number 36C25526Q0567, was posted on August 3, 2026, with responses due by August 10, 2026. It falls under NAICS code 611430 and is managed by the Department of Veterans Affairs through the 255-NETWORK Contract Office 15 located in Leavenworth, Kansas. Performance of services is expected to occur at the Kansas City, Missouri facility. The primary point of contact for inquiries is Kelly Malec, reachable via email at Kelly.Malec@va.gov. This sources sought notice is not an invitation to bid but a planning tool to determine the pool of qualified vendors capable of meeting the specified training requirements.
Professional and Management Development Training

POSTED

about 14 hours ago

DEADLINE

in 7 days
View Details