European Parliament and Council Regulation (EC)726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency [Agency for the Evaluation of Medicinal Products]. Adopted 31 March 2004.
Type
European material produced by EU institutions
Reference
OJL 136
Medicines for Human Use (Marketing Authorisations etc.) Amendment Regulations 2008
Monday, 8 December 2008
Statutory instruments
House of Lords
House of Commons
Monday, 8 December 2008
Statutory instruments
House of Lords
House of Commons
EC documents
14591/2001/1;14591/2001;15793/2002;10449/2003;REG(EC)726/2004;24643
Subjects
Published by
Not specified
Librarians' tools
Timestamp
2013-11-21 22:35:09 +0000
URI
http://esid.parliament.uk/EUDocument/EUMaterialPimsDocument/1575/
In Indexing
http://indexing.parliament.uk/Content/Edit/1?uri=http://esid.parliament.uk/EUDocument/EUMaterialPimsDocument/1575/
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Internal location
http://esid.parliament.uk/EUDocument/EUMaterialPimsDetails/1575/