Guidance

Electronic issue of blood components

Guidance for hospital blood banks on issuing blood components electronically in line with best practice.

From:
Medicines and Healthcare products Regulatory Agency
Published
6 May 2010

Documents

PDF, 54 KB, 3 pages

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Details

This guidance from the Medicines and Healthcare products Regulatory Agency (MHRA) clarifies the MHRA’s expectations on the control of electronic issue of blood components.

It should be used in conjunction with:

  • , referencing Commission Directive 2005/62/EC ‘standards and specifications relating to a quality system for blood establishments’

Updates to this page

Published 6 May 2010

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