Assembleia da República

Dossier COD/2008/0255

Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending, as regards information to the general public on medicinal products for human use subject to medical prescription, Regulation (EC) No 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

Subsidiarity deadline: 09/04/2012
 
Scrutiny Information

Scrutiny date: 04/04/2012

Subsidiarity Concern:

No Important information to exchange

No Veto

Information on parliamentary scrutiny

The draft act was scrutinised by the Health Committee (HC) and the HC's report has been forwarded to the European Affairs Committee.
T
he draft legislative act was scrutinised by the European Affairs Committee (EAC). The EAC’s written opinion does not raise any subsidiary issues and therefore the scrutiny procedure is concluded at the Portuguese Parliament.


Contact points for EU matters

IPEX Correspondents:
Phone: +351 21 391 08 46  Email Ms. Catarina Lopes
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