# Commission Regulation (EC) No 507/2006 of 29 March 2006 on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance) (revoked)

EU Regulation No 507/2006 · adopted 29 March 2006

Commission Regulation (EC) No 507/2006 of 29 March 2006 on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance)

## Introductory text

Commission Regulation (EC) No 507/2006
of 29 March 2006
on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council
(Text with EEA relevance) (revoked)
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## 1 Subject matter

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## 2 Scope

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## 3 Requests or proposals

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## 4 Requirements

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## 5 Specific obligations

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## 6 Renewal

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## 7 Marketing authorisation not subject to specific obligations

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## 8 Product Information

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## 9 Periodic safety update reports

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## 10 Agency advice prior to marketing authorisation application

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## 11 Guidelines

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## 12 Transitional provision

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## 13 Entry into force

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## Signature

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Source: https://www.legislation.gov.uk/eur/2006/507 (the official version)
Page: https://openlegislation.uk/eu-regulation-2006-507
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.