Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 Agenday and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (10324/EU XXIV.GP)

EU-V: Berichte u. Beratungsergebnisse

Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 Agenday and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use

Eingelangt am 03.04.2009, Bundesministerium für Gesundheit

RAT: 7996/09

Datum	EU-Datenbanknr.	Dokument der EU-Vorlage	Sprache	Einstufung
18.05.2009	12523/EU XXIV.GP	RAT: 7996/09 REV 1	englisch	LIMITE	EU-Vorlage Berichte u. Beratungsergebnisse Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use Eingelangt am 18.05.2009, Bundesministerium für Gesundheit
02.07.2009	15348/EU XXIV.GP	RAT: 7996/09 REV 3	englisch	LIMITE	EU-Vorlage Berichte u. Beratungsergebnisse Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use Eingelangt am 02.07.2009, Bundesministerium für Gesundheit

Interinstitutionelle Zahl Der Link führt zu den einzelnen Dokumenten dieses Vorhabens.	Link
2008/0257 COD	Legislative Observatory
2008/0260 COD	Legislative Observatory

Dok.Nr. Dokumenten der EU-Institutionen zugeordnete, fortlaufende Nummer mit Jahreszahl, um diese eindeutig zu identifizieren.	Betreff
RAT: 17501/08	Commission Staff Working Document accompanying document to the Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 and the Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use Impact Assessment (4286/EU XXIV.GP)
RAT: 17502/08	Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (4295/EU XXIV.GP)
RAT: 7015/09	Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (8779/EU XXIV.GP)

Code	Sachgebiet
MI 121	Binnenmarkt
SAN 61	Gesundheit
ECO 39	Wirtschaftsfragen
ENT 77	Technische Handelshemmnisse
CODEC 421	Mitentscheidungsverfahren

Thema
Außenhandel und Zoll
Binnenmarkt und Wettbewerb
Gesundheitswesen
Institutionelle Fragen
Wirtschaft, Währung & Finanzen

Datum	Dok.Nr. Dokumenten der EU-Institutionen zugeordnete, fortlaufende Nummer mit Jahreszahl, um diese eindeutig zu identifizieren.	Art	Betreff
02.07.2009	RAT: 11576/09	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Proposal for a Regulation of the European Parliament and of the Council amending, as regards pharmacovigilance of medicinal products for human use, 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 and Proposal for a Directive of the European Parliament and of the Council amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (15352/EU XXIV.GP)

EU-V: Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse