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
25-58248CanadaSubmission Closed
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
Active Opportunities Like This One
General Info
Agency
Government of Canada → National Research Council of Canada
NAICS
541690 - Other Scientific and Technical Consulting ServicesView NAICS
Place of Performance
Canada, CANSet-Aside
NONE
Timeline
PhaseClosed
Submission Closed
Organization & Contact Information
Show more
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
Full Description
Show more
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.
