Skip to main content

Part of the book series: Developments in Hematology and Immunology ((DIHI,volume 36))

  • 93 Accesses

Abstract

The use of blood and blood components has contributed hugely to advances made in medicine and surgery but, as has been discovered, their use is certainly not without risk. Contaminated blood and components can transmit disease and, as our knowledge increases, more risks can be identified.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. WHO Expert Committee on Biological Standardisation, WHO Technical Report Series 840, 1994.

    Google Scholar 

  2. Guide to the Preparation, Use and Quality Assurance of Blood Components, Council of Europe Publishing, Strasbourg, France. 6th Edition, 2000.

    Google Scholar 

  3. Commission of the European Communities. The Rules Governing Medicinal Products in the European Community Vol IV Good Manufacturing Practice for Medicinal Products, Luxembourg: Office for Official Publications of the EC, 1992.

    Google Scholar 

  4. Guidelines for the Blood Transfusion Services in the United Kingdom, The Stationery Office, London: 4th Edition, 2000.

    Google Scholar 

  5. PIC/S GMP Guide for Blood Centres (Draft).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2001 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Kavanagh, M.L. (2001). Legal and Regulatory Aspects of Blood Transfusion. In: Sibinga, C.T.S., Cash, J.D. (eds) Transfusion Medicine: Quo Vadis? What Has Been Achieved, What Is to Be Expected. Developments in Hematology and Immunology, vol 36. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1735-1_6

Download citation

  • DOI: https://doi.org/10.1007/978-1-4615-1735-1_6

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-5700-1

  • Online ISBN: 978-1-4615-1735-1

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics