Institutional and infrastructure challenges for hospitals producing advanced therapies in the UK: the concept of ‘point-of-care manufacturing readiness'

Edison Bicudo*, Irina Brass

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Aim: To propose the concept of point-of-care manufacturing readiness for analyzing the capacity that a country, a health system or an institution has developed to manufacture therapies in clinical settings (point-of-care manufacture). The focus is on advanced therapies (cell, gene and tissue engineering therapies) in the UK. Materials & methods: Literature review, analysis of quantitative data, and qualitative interviews with professionals and practitioners developing and administering advanced therapies. Results: Three components of point-of-care manufacturing readiness are analyzed staff and institutional procedures, infrastructure, and relations between hospitals and service providers. Conclusion: The technical and regulatory experience that has been gained through manufacturing advanced therapies at small scale in hospitals qualifies the UK for more complex and larger-scale production of therapies in the future.

Original languageEnglish
Pages (from-to)719-737
Number of pages19
JournalRegenerative medicine
Volume17
Issue number10
DOIs
Publication statusPublished - 1 Oct 2022

Bibliographical note

This work is licensed under the Attribution 4.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Keywords

  • advanced therapy medicinal products (ATMPs)
  • hospital exemption
  • institutional readiness
  • point-of-care manufacture
  • point-of-care manufacturing readiness
  • regulation

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