More resources for the Commission Regulation (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance)
Original Print PDF of EU Official Journal Version
This PDF does not include any changes made by corrigenda.
Original Print PDF
This is the PDF of the original version as first adopted in the EU that was published in the EU official journal. It therefore does not include any changes made by corrigendum (correction slips) issued after it was published. Corrigendum if issued will be listed separately under 'More Resources' and will have been applied to the HTML version viewable via the content tab.
- Download 789kB
Associated Documents
There are no associated documents for this legislation.
In Force Information
This data is taken from the Document Information page on EUR-Lex. Some of the terminology may differ from that used for UK legislation.
| Date of document | 03/08/2012 | ||
|---|---|---|---|
| Date of effect | 24/08/2012 | Entry into force | Date pub. + 20 See Art 3 |
| Date of effect | 02/11/2012 | Application | See Art 3 |
| Date of effect | 04/08/2013 | Application | Partial application Art 1 P.10 - P.15 - P.18.A - P.18.C - P.21 - P.22 - P.23 See Art 3 |
List of all changes :
- Affecting the Commission Regulation (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance)
- Made by the Commission Regulation (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance) affecting other Legislation
