Environmental monitoring of current good manufacturing practices cleanroom facilities for manufacturing of cellular therapy products in an academic hospital setting

Author:

Tanna JayORCID,McCann Chase D.ORCID,Smith Rhonda,Pitino AdrianaORCID,Asgedom Almaz,Kong Srey Leap,Weiner You LianORCID,Bushnell Kathryn,Webb JenniferORCID,Hanley Patrick J.ORCID

Funder

National Institutes of Health

Publisher

Elsevier BV

Reference25 articles.

1. Approved cellular and gene therapy products (updated 03/28/2024). Accessed 04/24/2024.https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-products/approved-cellular-and-gene-therapy-products.

2. FDA Statement from Commissioner of Food and Drug Administration Scott Gottlieb M.D. 2019. Accessed 07/13/2023.https://www.fda.gov/news-events/press-announcements/statement-fda-commissioner-scott-gottlieb-md-and-peter-marks-md-phd-director-center-biologics.

3. Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals,2023

4. Guidance for Industry. Sterile Drug Products Produced by Aseptic Processing,2004

5. General chapter, <1046>cell-based advanced therapies and tissue-based products,2023

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