# Commission Regulation (EC) No 668/2009 of 24 July 2009 implementing Regulation (EC) No 1394/2007 of the European Parliament and of the Council with regard to the evaluation and certification of quality and non-clinical data relating to advanced therapy medicinal products developed by micro, small and medium-sized enterprises (Text with EEA relevance) (revoked)

EU Regulation No 668/2009 · adopted 24 July 2009

Commission Regulation (EC) No 668/2009 of 24 July 2009 implementing Regulation (EC) No 1394/2007 of the European Parliament and of the Council with regard to the evaluation and certification of quality and non-clinical data relating to advanced therapy medicinal products developed by micro, small and medium-sized enterprises (Text with EEA relevance)

## Introductory text

Commission Regulation (EC) No 668/2009
of 24 July 2009
implementing Regulation (EC) No 1394/2007 of the European Parliament and of the Council with regard to the evaluation and certification of quality and non-clinical data relating to advanced therapy medicinal products developed by micro, small and medium-sized enterprises
(Text with EEA relevance) (revoked)
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## 1 Scope

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## 2 Procedure for evaluation and certification

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## 3 Site visits

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## 4 Combined advanced therapy medicinal products

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## 5 Scientific guidelines

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## 6 Report

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## 7 

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## Signature

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Source: https://www.legislation.gov.uk/eur/2009/668 (the official version)
Page: https://openlegislation.uk/eu-regulation-2009-668
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

