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This Solicitation opportunity from Government of Canada was posted on January 31, 2025. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

RFP - Manufacture and Supply of Buffered Diluent containing Glycerol and Sterile Empty Vials with Cap Enclosure

Closed
WS4617512505International

Contract Overview

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

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NAICS: 325412
New
Federal
6505--VA Loma Linda FDG
Solicitation # 36C26227Q0133
The Department of Veterans Affairs Loma Linda Healthcare System is conducting a Sources Sought and Request for Information (RFI) to identify qualified sources for a future single-award, Firm Fixed-Price Indefinite Delivery Indefinite Quantity (IDIQ) contract. The scope of work involves the procurement of radiopharmaceutical supplies, specifically 18-FDG, F18 NaF, and Bulk F-18 FDG. The intended period of performance consists of a base year starting December 15, 2026, followed by four option years ending December 14, 2031. The government is seeking providers capable of delivering sterile doses for intravenous injection that are compatible with the NMIS System and meet strict quality standards, including a radioactivity variance no greater than plus or minus 20 percent at the time of calibration. Deliveries will be made to the Nuclear Medicine Section at the Loma Linda facility, with routine orders required by the next business day and emergency orders required on the same day. The contractor must be licensed by the State of Operation and the Nuclear Regulatory Commission or an Agreement State Agency, and delivery personnel must be trained in Department of Transportation requirements and radiation safety. Interested parties must submit a capabilities statement, business size representations under NAICS 325412, and SAM.gov entity information to [email hidden] by November 20, 2026. This notice is for planning purposes only and does not constitute a formal solicitation.
262-NETWORK Contract Office 22 (36C262)

POSTED

about 23 hours ago

DEADLINE

in 6 days

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The Government of Canada, through the Department of Public Works and Government Services, is seeking a contractor to manufacture and supply critical medical countermeasures for its public health emergency stockpile. The requirement consists of 73,500 vials of a sterile 0.2% phenol, phosphate-citrate based buffered diluent containing 45% glycerol in 2 mL labelled vials, along with 11,000 empty 2 mL labelled sterile glass vials featuring a removable cap enclosure system capable of being re-stoppered. All products must be manufactured in accordance with Canada's Food and Drug Regulations, specifically Part C, Division 2 current Good Manufacturing Practices, to ensure they are of sufficient quality for human use. This solicitation, numbered WS4617512505, was posted on January 31, 2025, with a response deadline of February 20, 2025. Performance of the contract is associated with the National Capital Region.

General Info

Canada seeks a contractor for medical diluents and sterile vials for emergency stockpiles.

Documents

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Timeline

1 update
PhaseClosed
Posted

Solicitation

Notice updated

Response deadline changed from Jul 3, 2024 to Feb 20, 2025. The notice title changed. The notice description changed.

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyGovernment of Canada → Department of Public Works and Government Services
Contacts1 person available
OfficeN/A

Full Description

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Canada must procure and maintain a stockpile of medical countermeasures (MCM), including diluent and sterile empty glass vials required for vaccination, to support response to Canadian public health emergencies and events. The Government of Canada has a requirement for the services of a Contractor to manufacture and supply 73,500 vials of a sterile 0.2% phenol, phosphate-citrate based buffered diluent containing 45% glycerol (pH 7.4) in 2 mL labelled vials, accompanied by 11,000 empty 2mL labelled sterile glass vials with a removable cap enclosure system capable of being re-stoppered, in accordance with the technical specifications set out in Appendix A of this solicitation. The diluent and empty vials must be manufactured in accordance with Canada’s Food and Drug Regulations, Part C, Division 2 - current Good Manufacturing Practices (GMP), and be of sufficient quality for use in humans.

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