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Essential requirements for setting up a stem cell processing laboratory

Identifieur interne : 000333 ( France/Analysis ); précédent : 000332; suivant : 000334

Essential requirements for setting up a stem cell processing laboratory

Auteurs : T. Leemhuis [États-Unis] ; D. Padley [États-Unis] ; C. Keever-Taylor [États-Unis] ; D. Niederwieser [Allemagne] ; T. Teshima [Japon] ; F. Lanza [Italie] ; C. Chabannon [France] ; P. Szabolcs [États-Unis] ; A. Bazarbachi [Liban] ; M. B. C. Koh [Royaume-Uni, Singapour]

Source :

RBID : Pascal:14-0231456

Descripteurs français

English descriptors

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.


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Pascal:14-0231456

Le document en format XML

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<div type="abstract" xml:lang="en">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.</div>
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