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Supply of Legionella Urine Antigen Test Kits

Active
International

Contract Overview

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

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This subcontract involves the manufacture, packaging, and delivery of specialized Legionella pneumophila urine antigen test kits for prime contractors serving Public Health Ontario. The supplier is responsible for utilizing specific diagnostic reagents and antigen-capture antibodies to produce validated medical diagnostic kits. To be eligible, the provider must hold medical device regulatory certification from Health Canada, the FDA, or an equivalent recognized diagnostic standard. The contract is managed under the Government of Ontario through the OAHPP, with a focus on the physical shipment of these kits to designated facilities. Interested parties must respond by October 5, 2026, in accordance with NAICS code 325413.

General Info

Manufacture and deliver Legionella test kits for Public Health Ontario by October 5, 2026.

Agency

Government of Ontario → OAHPP (Public Health Ontario)View Agency

NAICS

325413 - In-Vitro Diagnostic Substance ManufacturingView NAICS

Place of Performance

ON, CAN

Set-Aside

NONE

Documents

This scope was carved out of rfi_2019.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

163627001 ACAN - Legionella Urine Antigen Test Kits

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Timeline

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Organization & Contact Information

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AgencyGovernment of Ontario → OAHPP (Public Health Ontario)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Government of Ontario → OAHPP (Public Health Ontario)
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Office AddressN/A
ContactsNo contact information available

Full Description

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Supplies specialized medical diagnostic kits for prime contractors delivering to Public Health Ontario. Manufactures, packages, and delivers validated urine antigen test kits using diagnostic reagents and antigen-capture antibodies specific to Legionella pneumophila. Requires medical device regulatory certification from Health Canada, FDA, or equivalent diagnostic standards. Delivers physical shipments of test kits to designated facilities.

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