6.13: References

1. Council of Europe (2023). Guide for the Preparation, Use and Quality Assurance of Blood Components, 21st edition. Council of Europe Publishing.
2. Beckman N, Nightingale MJ, Pamphilon D (2009). Practical guidelines for applying statistical process control to blood component production. Transfusion Medicine, 19, 329–339.
3. Medicines and Healthcare products Regulatory Agency (2022). Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Orange Guide) 2022. London: Pharmaceutical Press.
4. Nightingale MJ, Lees B, Biset R, Mertens W (2006). Use of a (proposed) standard protocol to validate Terumo TSCD-II connections between dissimilar blood bag tubing. Vox Sanguinis, 91, 241–269.
5. Nightingale MJ, De Korte D, Chabenel A, Hughes W, Rowe GP, Nicholson G (2011). Eurobloodpack: a common European design for blood bag systems with integral leucodepletion filters. Vox Sanguinis, 101, 250–254.
6. Department of Health: Health Technical Memorandum 07-01: Safe Management of Healthcare Waste. Published by TSO (The Stationery Office) 2013. https://www.england.nhs.uk/publication/management-and-disposal-of-healthcare-waste-htm-07-01
7. UK Blood Safety and Quality Regulations (BSQR). Available at www.legislation.gov.uk/uksi/2005/50. BSQR amendments available at www.legislation.gov.uk/uksi/2005/2898 and www.legislation.gov.uk/uksi/2006/2013