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Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22: Difference between revisions

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authorisation and supervision of medicinal products for human use  28-Jan-22
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authorisation and supervision of medicinal products for human use
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|reference=EU  Regulation (EC) No 726/2004 -  
authorisation and supervision of medicinal products for human use  28-Jan-22
authorisation and supervision of medicinal products for human use  28-Jan-22
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== References ==
{| class="wikitable"
! Reference !! Scope !! Document part !! Language !! Preview
|-
| [[Reference:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 Article 26]] || NIS || Article 26 || EN || Article 26 1. The Agency shall, in collaboration with the Member States and the Commission, set up and maintain a European medicines web-portal [EU PAS Register] for the dissemination of information ...
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Latest revision as of 14:15, 16 July 2026


Document information
Reference EU Regulation (EC) No 726/2004 -

authorisation and supervision of medicinal products for human use 28-Jan-22

Validity area EU
Scope(s) NIS
Document name Regulation (EC) No 726/2004 -

authorisation and supervision of medicinal products for human use

Version / Revision 28-Jan-22
Status Current
Document type Legal act
Language(s) EN
Description Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)
Official source Official link
Restricted access No
Submitted by Florian Adragna
Contributors

References

 ScopeDocument partLanguagePreview
EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 Article 26NISArticle 26ENArticle 26 1. The Agency shall, in collaboration with the Member States and the Commission, set up and maintain a European medicines web-portal [EU…
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