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Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology) 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024

Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology)
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简体网页||繁体网页
Sibinga, C. Th Smit; Sibinga; Smit Sibinga, C. Th 作者
Springer
译者
1994-08-31 出版日期
313 页数
USD 179.00 价格
Hardcover
丛书系列
9780792330097 图书编码

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Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology) 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology) 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology) 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024


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Good Manufacturing Practice in Transfusion Medicine (Developments in Hematology and Immunology) 在线电子书 图书描述

Transfusion medicine provides an excellent bridge connecting the healthy community donors with the patient's needs at the bedside; the dominant philosophy has been on patient care and science, but it is now realised that blood banks manufacture increasing amounts of blood components to administer to patients -- a role analogous to manufacturing functions. The concept of Good Manufacturing Practice (GMP) is therefore relatively new. While quality has always been important, the impact of GMP, Total Quality Management (TQM) and Quality Assurance (QA) will be profound. As the regulatory agencies, like the FDA in the U.S.A. and the EEC Commission in Europe, increase their enforcement activities, doctors, technical experts and managers will have to face many issues of quality assurance including documentation, validation, audit system, regulatory laws, licensing, teaching and training of staff and their job descriptions, standards, processing facilities, procedure validations, automation, record keeping, internal and external quality control of products and their release. The expansion of this philosophy to include Good Clinical Practice (GCP) is an even greater challenge demanding consensus therapy protocols and quality management of transfusion through auditing by the hospital transfusion committees. Such comprehensive plans will profoundly affect the financial and organisational structure of blood transfusion in the future.

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