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 (17300/EU XXIV.GP)

RAT: 12421/09 LIMITE
24.08.2009
englisch

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

Eingelangt am 24.08.2009, Bundesministerium für Gesundheit (Abteilung I/5)

 Einklappen
Datum EU-Datenbanknr. Dokument der EU-Vorlage Sprache Einstufung
01.10.2009 19144/EU XXIV.GP
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 01.10.2009, Bundesministerium für Gesundheit

04.11.2009 21477/EU XXIV.GP
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 proecedures 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 04.11.2009, Bundesministerium für Gesundheit

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Interinstitutionelle Zahl
Link
2008/0257 COD
2008/0260 COD
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Dok.Nr.
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: 11576/09 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 (15352/EU XXIV.GP)
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Code Sachgebiet
MI 285 Binnenmarkt
SAN 203 Gesundheit
ECO 102 Wirtschaftsfragen
ENT 162 Technische Handelshemmnisse
CODEC 1017 Mitentscheidungsverfahren
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