Establishing the variation of blood metrics within UK Biobank to inform cell therapy manufacturing processes
Author:
Affiliation:
1. Centre for Biological Engineering, Loughborough University, Loughborough, Leicestershire, LE11 2QZ, UK
Abstract
Publisher
Future Medicine Ltd
Subject
Embryology,Biomedical Engineering
Link
https://www.futuremedicine.com/doi/pdf/10.2217/rme-2018-0168
Reference18 articles.
1. Scanning the horizon for high value-add manufacturing science: Accelerating manufacturing readiness for the next generation of disruptive, high-value curative cell therapeutics
2. European Commission. EudraLex– The rules governing medicinal products in the European Union, volume 4, good manufacturing practice, guidelines of 22.11.2017: good manufacturing practice for advanced therapy medicinal products. Brussels, Belgium 22.11.2017 C(2017) 7694 Final, (2017). https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-4/2017_11_22_guidelines_gmp_for_atmps.pdf
3. Balancing Safety and Innovation for Cell-Based Regenerative Medicine
4. Automating decentralized manufacturing of cell & gene therapy products
5. Decentralized manufacturing of cell and gene therapies: Overcoming challenges and identifying opportunities
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