Accommodating clinical trials and other externally manufactured cellular therapy products: challenges, lessons learned and creative solutions-Reference-Cited by-同舟云学术

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Accommodating clinical trials and other externally manufactured cellular therapy products: challenges, lessons learned and creative solutions

Published:2022-01 Issue:1 Volume:24 Page:37-44
ISSN:1465-3249
Container-title:Cytotherapy
language:en
Short-container-title:Cytotherapy

Author:

Jackson Matthew R.

Publisher

Elsevier BV

Subject

Cancer Research,Transplantation,Cell Biology,Genetics (clinical),Oncology,Immunology,Immunology and Allergy

Reference2 articles.

1. Seventh Edition FACT-JACIE Hematopoietic Cellular Therapy Accreditation Manual. (2018). FOUNDATION FOR THE ACCREDITATION OF CELLULAR THERAPY (FACT).

2. Code of Federal Regulations, 21 U.S.C., §1271 (2001).

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Successful transport across continents of GMP-manufactured and cryopreserved culture-expanded human fetal liver-derived mesenchymal stem cells for use in a clinical trial;Regenerative Therapy;2024-06

2. Remote audit practice for inspection of structural and equipment standards for cell processing facilities under the act on the safety of regenerative medicine in Japan;Regenerative Therapy;2024-03

3. Integrating Artificial Intelligence for Academic Advanced Therapy Medicinal Products: Challenges and Opportunities;Applied Sciences;2024-02-05

4. Healthcare center‐based cell therapy laboratories supporting off‐site manufactured cell therapies: The experiences of a single academic cell therapy laboratory;Transfusion;2024-01-03

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