# Commission Directive 2006/86/EC of 24 October 2006 implementing Directive 2004/23/EC of the European Parliament and of the Council as regards traceability requirements, notification of serious adverse reactions and events and certain technical requirements for the coding, processing, preservation, storage and distribution of human tissues and cells (Text with EEA relevance), Division PART B: Conclusions of Serious Adverse Events investigation

Extent: E+W+S+N.I.

Tissue establishment
EU tissue establishment code (if applicable)
Report identification
Confirmation date (year/month/day)
Date of serious adverse event (year/month/day)
Root cause analysis (details)
Corrective measures taken (details)

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Source: https://www.legislation.gov.uk/eudr/2006/86/annex/IV/part/B (the official version)
Page: https://openlegislation.uk/eu-directive-2006-86/annex-IV/part-B
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.