Formation opérationnelle personnalisée et appliquée en fabrication biopharmaceutique conforme aux bonnes pratiques de fabrication (BPF).
Résumé public
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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.
Aperçu des exigences
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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.
Aperçu de la description source
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Le Conseil national de recherches du Canada (CNRC)doit se procurer les services suivants : l’Installation de matériel pour essais cliniques (IMEC) a besoin d’une formation opérationnelle avancée et personnalisée en fabrication biopharmaceutique conforme aux bonnes pratiques de fabrication (BPF). Cette formation doit être pratique et réalisée à l’aide d’équipements comparables à ceux utilisés à l’Installation de matériel pour essais cliniques (IMEC) du CNRC, c’est- à-dire dans un environnement de salle blanche conforme aux BPF.
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