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 language | English |
|---|---|
| Pages (from-to) | 719-737 |
| Number of pages | 19 |
| Journal | Regenerative medicine |
| Volume | 17 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 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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