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Validation Services for a new Clinical Trial Manufacturing Facility (CTMF) | National Research Council Canada · CanPursue
Opportunities
Fit is part of the trial and paid plans.Closed

Validation Services for a new Clinical Trial Manufacturing Facility (CTMF)

National Research Council Canada22-58009Federal
Find on CanadaBuysAdd to pipeline
Published
May 16, 2022
Respond by
Jun 9, 2022
Latest amendment
—6 amendments

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Description

The National Research Council of Canada is building a new Clinical Trial Manufacturing Facility (CTMF) thatwill house the process and equipment for the production and the quality control of protein, viral vectoror virus-like particle vaccines or biologics.The products are mainly intended for the Canadian market, regulated by Health Canada under theauthority of the Food and Drugs Act. The facility will require being compliant with Canadian GoodManufacturing Practices (GMP) as well as FDA current GMP (cGMP) and Eudralex requirements.The new manufacturing rooms and airlocks (personnel and material) will be built in an extension to theexisting NRC’s premises located in Montreal, Quebec and will consist of classified grade C and D areas.The facility will include equipment and infrastructures necessary for viral seed stock preparation,subculture, cell culture and viral production, purification and warehousing.

Procurement

Category
Services
Jurisdiction
Federal

Not stated in the notice: procurement type, procurement method, selection criteria, region of delivery, region of opportunity, expected contract period, end user

Requirements and qualifications

Supply arrangement
Not stated in the public notice
Security requirement
Not stated in the public notice
Trade agreements
—
Limited tendering reason
—

Classification

GSIN
—
UNSPSC
—

Amendments

The source reports 6 amendments. CanPursue observed 1 of them with dates.

  • Amendment 6Jun 1, 2022
  • Original noticeMay 16, 2022

Documents

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Source

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Source
CanadaBuys
Solicitation
22-58009
Observed
Sep 18, 2026

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