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This Solicitation opportunity from Government of Canada was posted on March 22, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Professional services - GMP Production Documentation and Technical Support consultant for Clinical Trial Material Facility (CTMF).

Closed
25-58248Canada

Contract Overview

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General Info

Agency

Government of Canada → National Research Council of Canada

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Canada, CAN

Set-Aside

NONE

Documents

(5)

RFP-25-58248_Amendment_2_ April_22_26.pdf

PDF

NPP_25-58248_CTMF_EN_FR_final.pdf

PDF

FINAL_RFP-25-58248_French_20_March_annexed_signed.pdf

PDF

RFP-25-58248_Modification –17 April__0.pdf

PDF

FINAL_RFP_25-58248_EN_March_20_annexed_signed.pdf

PDF

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Timeline

PhaseClosed
Posted

Solicitation

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyGovernment of Canada → National Research Council of Canada
Contacts1 person available
OfficeN/A
Organization / Agency
Government of Canada → National Research Council of Canada
Office AddressN/A
Contacts
Cindy RomainContracting Authority

Full Description

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Good Manufacturing Practices (GMP) consultant support to generate, review and approve production documentation (i.e. SOPs, logbooks, validation protocol IQ/OQ/PQ and reports, validation test scripts, study, deviation, CAPA, risk assessment, material code specification, change control). In addition, the consultant will act as a technical advisor to the production manager. This is a contract to support the production manager on the review of all related documentation for Data Integrity Assessment and Validation PQs. These activities are required to ensure that production can move forward with the CTMF projects for bulk drug product manufacturing beginning in April 2026.