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Publications CAN/CSA-Z902-15

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CAN/CSA-Z902-15 - Blood and blood components

Publication Year:

  • 2015

Total Pages:



  • CSA

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    Z900-12 PACKAGE

    Z900-12 PACKAGE - Consists of CAN/CSA-Z900.1-12, Cells, tissues, and organs for transplantation: General requirements; CAN/CSA-Z900.2.1-12, Tissues for assisted reproduction; CAN/CSA-Z900.2.2-12, Tissues for transplantation; CAN/CSA-Z900.2.3-12, Perfusable organs for transplantation; CAN/CSA-Z900.2.4-12, Ocular tissues for transplantation and CAN/CSA-Z900.2.5-12, Lymphohematopoietic cells for transplantation

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    CAN/CSA-Z900.2.1-12 - Tissues for assisted reproduction

  • Sorry, no image available for CANCSA-Z900.2.4-12



    CAN/CSA-Z900.2.4-12 - Ocular tissues for transplantation

  • Sorry, no image available for CAN/CSA-Z900.1-12



    CAN/CSA-Z900.1-12 - Cells, tissues, and organs for transplantation: General requirements

  • Sorry, no image available for CAN/CSA-Z900.2.5-12



    CAN/CSA-Z900.2.5-12 - Lymphohematopoietic cells for transplantation

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For More Information:


The third edition of CSA Z902 provides management requirements for facilities that collect, process, store, and use human blood components for transfusion. It helps to protect recipients of blood and blood components as well as personnel and others who are exposed to blood and blood components by addressing safety, efficacy and quality issues.

First published in 2004, this management standard applies to any organization that collects, processes, stores, or uses human blood components for transfusion and is a valuable tool to assist in the preparation of detailed specifications and operating procedures. Organizations that manage blood products but not blood components (e.g., a hospital pharmacy), are encouraged to review the relevant requirements for blood products and incorporate them as appropriate into their procedures.

Highlights of Z902

  • Includes requirements for policies and procedures, quality management, personnel, physical plant, and equipment
  • Outlines specific requirements to be included in the facilityís operating procedures for many critical activities including but not limited to: donor selection for allogeneic blood collection; collection of blood components for transfusion; preparation of blood components; testing and labelling of blood components; home transfusion; and records management
  • Includes informative annexes, tables and figures

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