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- W1505308557 abstract "There continue to be many developments in cellular therapy encompassing the transplantation of haemopoietic progenitor cells (HPC), immunotherapy with cells of the lymphoid system and cells for tissue repair and regenerative medicine. The environment of cellular therapy is a highly regulated one, aiming to ensure high quality and microbiological safety, and this has led to the introduction of both voluntary accreditation systems and compulsory regulations at both national and international level. Compulsory requirements include those of the European Union Directives and the US Food and Drug Administration (FDA), whereas voluntary accreditation of HPC transplant programmes, including collection and processing facilities, is administered by FACT and JACIE while AABB and the College of American Pathologists (CAP) accredit exclusively collection and processing facilities. Netcord and FACT as well as AABB accredit CB collection and laboratory facilities. Tissue typing services are accredited via European or American bodies (EFI and ASHI), as well as the College of American Pathologists. Donor registries are typically members of the World Marrow Donor Association (WMDA) accreditation scheme. The development of quality systems is central to compliance with regulatory and accreditation requirements." @default.
- W1505308557 created "2016-06-24" @default.
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- W1505308557 date "2013-02-26" @default.
- W1505308557 modified "2023-09-23" @default.
- W1505308557 title "Regulation and Accreditation in Cellular Therapy" @default.
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- W1505308557 doi "https://doi.org/10.1002/9781118520093.ch38" @default.
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