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Human- und Tierarzneimittel/Europäische Arzneimittelagentur/Pharmakovigilanz von Humanarzneimitteln (33636/EU XXIV.GP)

  • RAT: 10779/10 LIMITE
  • 23.06.2010
  • englisch

Übersicht

EU-Vorlage Berichte u. Beratungsergebnisse

Rat A/I-Punkt-Vermerk

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

Dokument der EU-Vorlage: RAT: 10779/10 

Gegenstandsgleiche Dokumente

Datum EU-Datenbanknr. Dokument der EU-Vorlage Sprache Einstufung
Alle aufklappen
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

Schließen
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

Schließen
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

Schließen
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

Schließen

Interinstitutionelle Dossiers

Referenzierte Dokumente

Sachgebiete des Rates

Code Sachgebiet
MI 200 Binnenmarkt
SAN 133 Gesundheit
ECO 44 Wirtschaftsfragen
ENT 67 Technische Handelshemmnisse
CODEC 531 Mitentscheidungsverfahren

Zugeordnete Themen

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