Reducing Microbial Contamination in Hematopoietic Stem Cell Products and Quality Improvement Strategy: Retrospective Analysis of 1996-2021 Data-Reference-Cited by-同舟云学术

Reducing Microbial Contamination in Hematopoietic Stem Cell Products and Quality Improvement Strategy: Retrospective Analysis of 1996-2021 Data

Published:2023-04-21 Issue:5 Volume:43 Page:477-484
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Ko You Keun¹²^ORCID,Lee Jong Kwon¹²^ORCID,Park Hye Kyung¹³^ORCID,Han Ae Kyung¹^ORCID,Mun Sun Kyoung¹^ORCID,Park Hye Jeong¹^ORCID,Choung Hae Kyoung¹^ORCID,Kim Se Mi¹^ORCID,Choi Kwang Mo¹^ORCID,Lee Nam Yong¹²^ORCID,Cho Duck¹²³^ORCID,Kim Dae Won⁴^ORCID,Kang Eun-Suk¹²³^ORCID

Affiliation:

1. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

2. Department of Laboratory Medicine and Genetics, School of Medicine, Sungkyunkwan University, Suwon, Korea

3. Cell and Gene Therapy Institute, Research Institute for Future Medicine, Samsung Medical Center, Seoul, Korea

4. Department of Laboratory Medicine, Korea University Anam Hospital, Seoul, Korea

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

http://pdf.medrang.co.kr/ALM/2023/043/alm-43-5-477.pdf

Reference33 articles.

1. The role of the EBMT activity survey in the management of hematopoietic stem cell transplantation

2. One million haemopoietic stem-cell transplants: a retrospective observational study

3. Microbiological control in stem cell banks: approaches to standardisation

4. Liquid Storage of Hematopoietic Stem Cells Versus Proliferative Potential Colony-Forming Unit Granulocyte-Monocytes: Validation of Cell Processing

5. Risk Analysis of Hematopoietic Stem Cell Transplant Process: Failure Mode, Effect, and Criticality Analysis and Hazard Analysis Critical Control Point Methods Integration Based on Guidelines to Good Manufacturing Practice for Medicinal Product ANNEX 20 (February 2008)

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