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Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin (Text with EEA relevance)
Annex I

Division 1 RISK ANALYSIS AND RISK MANAGEMENT

United Kingdom

Original text. Later amendments are not shown.

1.1Justification for the use of animal tissues or derivatives
1.2Process of risk assessment
1.3Review of the risk assessment

Division 1

Division 1.1 →

Legislation: Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin (Text with EEA relevance)
Citation: EU Regulation No 722/2012, division 1
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright
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