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Commission Implementing Regulation (EU) No 198/2013 of 7 March 2013 on the selection of a symbol for the purpose of identifying medicinal products for human use that are subject to additional monitoring Text with EEA relevance

Basic information

In force
CELEX number: 32013R0198
Official Journal: JOL_2013_065_R_0017_01
Form: Regulation
Procedure number: --
Languages:
- bg
- cs
- da
- de
- el
- en
- et
- fi
- fr
- hr
- hu
- it
- lv
- lt
- mt
- nl
- pl
- pt
- ro
- sk
- sl
- es
- sv

Dates

Date of document:

March 7, 2013

Date of publication:

March 8, 2013

Date of effect:

March 28, 2013
- Entry into force - Date pub. +20 See Art 4

Modified by

Amendment proposed by:

Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006

Modifies

Affected by case

Legal basis

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)

EuroVoc Vocabulary

Health control
Market approval
Consumer information
Public health
Medicinal product
Internal market - Principles
Labelling
Health protection
Medicinal products
Proprietary medicinal products