Aug 5, 2026
Closes
Aug 17, 2026
Intrusion Detection System Services - Request for Quote
Installment of intrusion detection system (ids) and monitoring services.
Description: The contractor shall procure and provide to Customs and Border Protection (CBP) canines that are suitable for training. CBP has the option to procure up to 25% for additional canines from the RFQ stated quantity. a. Canines are required to be in-place no-later-than 30-days from award notification by the contracting Officer. b. The contractor has 60-days after each receipt of notification of non-acceptance to furnish a replacement canine(s). After 150-days of award notification, CBP reserves the right to terminate any outstanding portion(s) of the order. Vendors who have been terminated for any outstanding part of their order will not be eligible for the re-compete orders. c. Any canine(s) that fails to pass the requirements or physical testing performed by CBP will not be accepted; the contractor will bear all expenses associated with the return of the canine to the contractor’s site within 7-days after receiving notification. See attached file.
Federal · DC, US
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Procurement and program contacts connected to U.S. Customs and Border Protection.
These related opportunities are still open for bidding.
Aug 5, 2026
Closes
Aug 17, 2026
Installment of intrusion detection system (ids) and monitoring services.
CityPA
Aug 1, 2026
Closes
Sep 28, 2026
Veterinary services for approx. 40 canines, veterinary facilities for an annual veterinary plan for the City’s canines.
Aug 3, 2026
Closes
Sep 2, 2026
To gather detailed insights from companies and consortia engaged in the engineering, testing, and manufacturing of medical device prototypes relevant to the detection of human cyanide exposure. DHS seek collaborator(s) with expertise in chemical medical countermeasures, particularly those that can demonstrate a robust background in developing detection technologies for hazardous substances, including past projects and relevant experience. Responses should outline the engineering and design processes utilized in creating prototypes, including biomarker selection and validation methodologies, as well as comprehensive cost estimates and timelines for development from proof of concept through regulatory approval and manufacturing. Additionally, respondents should provide information on navigating the regulatory landscape for medical devices, including experience with agencies like the Food and Drug Administration (FDA), and detail their manufacturing capabilities, including scalability and compliance with industry standards. See attached file.
West Virginia General Services Division
State AgencyWV
Aug 6, 2026
Closes
Aug 20, 2026
Graykey online advanced software or equal.