| Location: | Federal |
|---|---|
| Posted: | Feb 11, 2026 |
| Due: | Mar 24, 2026 |
| Agency: | Government of Canada |
| Type of Government: | State & Local |
| Category: |
|
| Solicitation No: | 25-58073 |
| Publication URL: | To access bid details, please log in. |
Description
The objective of the project is to have tests carried out in accordance with Good Manufacturing Practices
and current regulations (Health Canada, Food and Drug Administration (FDA), European Medicines
Agency (EMA) for the analysis of raw materials, solutions, products, etc., in order to confirm the quality of
our products.
The National Research Council of Canada has built a new Clinical Trial Material Facility (CTMF) that will
house the process and equipment for the production and the quality control of protein, viral vector or virus-
like particle vaccines or biologics. The facility will require being compliant with Canadian Good
Manufacturing Practices (GMP) as well as FDA current GMP (cGMP) and Eudralex requirements.
This supply Arrangement includes 3 Streams (1,2,3) of services as follows: Stream 1 – Raw Material Analysis , Stream 2 – Various solutions, Biological products Analysis and Stream 3 – Cell Bank Characterization . See Statement of work for full details.
The estimated contract period will be 60 month(s), with a proposed start date of 2026/04/15.
A contracting officer can use limited tendering for specific reasons outlined in the applicable trade agreements. The reason for this contract is described below:
Are you interested in partnering with other businesses for this opportunity? Add your company to the list of businesses who are interested in partnering .
This list does not replace or affect the tendering procedures for this procurement process. Businesses are still required to respond to bid solicitations, and to compete based on the set criteria. For more information please read the Terms of use .

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