Customized and applied Goods Manufacturing Practices (GMP) -Compliance Biomanufacturing Operational Training
Public summary
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The National Research Council of Canada (NRC) appears to be seeking customized, advanced Goods Manufacturing Practices (GMP) training for staff at its Clinical Trial Material Facility (CTMF) in Montreal, Quebec. The training is expected to be practical and hands-on, using equipment and conditions comparable to the facility’s GMP-compliant clean-room environment. The notice is currently listed as open and has a closing date of October 9, 2026, at 2:00 p.m. A business offering specialized GMP, biomanufacturing, clean-room, or clinical-trial-material training may find this opportunity potentially relevant, but the tender details should be reviewed carefully to confirm the required qualifications, delivery expectations, procurement process, and whether the notice is an advance contract award notice. Review the official documents before deciding whether to respond: https://canadabuys.canada.ca/sites/default/files/webform/tender_notice/108087/26-58172_acan_gmp_training_final_en.pdf and https://canadabuys.canada.ca/sites/default/files/webform/tender_notice/108087/npp_acan_26-58172_gmp_training_ctmf_25sept_en.pdf. Bid Maple is not affiliated with the Government of Canada, and all details should be verified against the official tender notice before submitting a bid or response.
Requirement preview
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- Provide customized and advanced Goods Manufacturing Practices (GMP)-compliant biomanufacturing operational training for the National Research Council of Canada’s Clinical Trial Material Facility (CTMF).
- Training must be hands-on and involve the use of equipment comparable to equipment used within NRC’s CTMF.
- Training must take place in a clean-room, GMP-compliant environment.
- The requirement is identified for Canada, Montreal, Quebec; confirm the precise delivery location in the official tender documents.
Source description preview
Imported source text may contain formatting from the original notice.
The Department of National Research Council (NRC) has a requirement to procure the following services the Clinical Trial Material Facility (CTMF) requires customized and advanced GMP- compliant biomanufacturing operational training. It must be hands-on use of equipment comparable to that used within NRC's Clinical Trial Material Facility (CTMF) i.e. a Clean Room, GMP compliant environment.
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