Tour Andover Controls Helps Héma-Québec Ensure Safe And Sufficient Blood Supplies
Source: TAC
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•Case Study: Tour Andover Controls Helps Héma-Québec Ensure Safe And Sufficient Blood Supplies
Blood processing establishments require strict compliance with internationally recognized safety standards pertaining to the collection, screening, preparation, and delivery of blood components. A key element of regulatory compliance is having a quality facility management system in place to control and monitor the environment in which blood is processed and stored.
•Case Study: Tour Andover Controls Helps Héma-Québec Ensure Safe And Sufficient Blood Supplies
•Case Study: Tour Andover Controls Helps Héma-Québec Ensure Safe And Sufficient Blood Supplies
Blood processing establishments require strict compliance with internationally recognized safety standards pertaining to the collection, screening, preparation, and delivery of blood components. A key element of regulatory compliance is having a quality facility management system in place to control and monitor the environment in which blood is processed and stored.
Héma-Québec, a leading Canadian blood supplier, must comply with standards established by Health Canada, the country's federally funded healthcare agency. In particular, Héma-Québec is subject to GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and GTHP (Good Tissue Handling Practices) regulations. To meet this challenge, they turned to ACS Montréal Inc. to install an Andover Continuum® Facility Management System with CFR Compliance Pack™. Continuum provides Héma-Québec with facilitywide accountability and traceability of the environmental conditions in their labs and donor centers.
Click Here To Download:
•Case Study: Tour Andover Controls Helps Héma-Québec Ensure Safe And Sufficient Blood Supplies
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