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 (LA) (first reading) - Approval of the final compromise text (33636/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 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 (LA) (first reading) - Approval of the final compromise text

Eingelangt am 23.06.2010, Bundesministerium für Gesundheit

RAT: 10779/10

Datum	EU-Datenbanknr.	Dokument der EU-Vorlage	Sprache	Einstufung
23.06.2010	33635/EU XXIV.GP	RAT: 10779/10 ADD 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 (LA) (first reading) - Approval of the final compromise text Eingelangt am 23.06.2010, Bundesministerium für Gesundheit
23.06.2010	33634/EU XXIV.GP	RAT: 10779/10 ADD 2	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 (LA) (first reading) - Approval of the final compromise text Eingelangt am 23.06.2010, Bundesministerium für Gesundheit
13.08.2010	35955/EU XXIV.GP	RAT: 10779/10 ADD 1 COR 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 (LA) (first reading) - Approval of the final compromise text Eingelangt am 13.08.2010, Bundesministerium für Gesundheit
13.08.2010	35954/EU XXIV.GP	RAT: 10779/10 COR 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 (LA) (first reading) - Approval of the final compromise text Eingelangt am 13.08.2010, 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: 9697/10

Code	Sachgebiet
MI 200	Binnenmarkt
SAN 133	Gesundheit
ECO 44	Wirtschaftsfragen
ENT 67	Technische Handelshemmnisse
CODEC 531	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
22.06.2010	NON: 1560/10	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Bericht der Ständigen Vertretung über die Sitzung Mertens-Gruppe vom 22.6.2010 (33583/EU XXIV.GP)

EU-V: Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse

EU-Vorlage Berichte u. Beratungsergebnisse