Essential requirements for setting up a stem cell processing laboratory

Abstract

The Graft Processing subcommittee of the Worldwide Network for Blood and Marrow Transplantation wrote this guideline to assist physicians and laboratory technologists with the setting up of a cell processing laboratory (CPL) to support a hematopoietic stem cell transplant program, thereby facilitating the start-up of a transplant program in a new location and improving patient access to transplantation worldwide. This guideline describes the minimal essential features of designing such a laboratory and provides a list of equipment and supply needs and staffing recommendations. It describes the typical scope of services that a CPL is expected to perform, including product testing services, and discusses the basic principles behind the most frequent procedures. Quality management (QM) principles specific to a CPL are also discussed. References to additional guidance documents that are available worldwide to assist with QM and regulatory compliance are also provided. © 2014 Macmillan Publishers Limited All rights reserved.

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Keywords

Hematopoietic stem cell transplantation, Hematopoietic stem cells, Humans, Laboratories, hospital, Medical laboratory personnel, Practice guidelines as topic, Reagent, Article, Cell processing laboratory, Cell therapy, Device safety, Good laboratory practice, Health care access, Health care availability, Hematopoietic stem cell, Laboratory, Laboratory device, Laboratory personnel, Medical technologist, Practice guideline, Priority journal, Process design, Program development, Protocol compliance, Scope of practice, Total quality management, Hospital laboratory, Human, Organization and management, Standards, Supply and distribution

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