Guideline: EC/540/95 - Commission Regulation (EC) No 540/95, of 10 March 1995, laying down the arrangements for reporting suspected unexpected adverse reactions which are not serious, whether arising in the Community or in a third country, to medicinal products for human or veterinary use authorized in accordance with the provisions of Council Regulation (EEC) No 2309/93.
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| Titel: | EC/540/95 - Commission Regulation (EC) No 540/95, of 10 March 1995, laying down the arrangements for reporting suspected unexpected adverse reactions which are not serious, whether arising in the Community or in a third country, to medicinal products for human or veterinary use authorized in accordance with the provisions of Council Regulation (EEC) No 2309/93. |
| Kurztitel: | EC/540/95 |
| Internet: | http://ec.europa.eu/health/files/eudralex/vol-1/reg_1995_540/reg_1995_540_en.pdf |
| Herkunft/Verlag: | European Commission, Enterprise and Industry; http://ec.europa.eu/enterprise/ |
| Inhalt: | Verordnung (EG) Nr. 540/95 der Kommission vom 10. März
1995 zur Festlegung der Bestimmungen für die Mitteilung von
vermuteten unerwarteten, nicht schwerwiegenden
Nebenwirkungen, die innerhalb oder außerhalb der
Gemeinschaft an gemäß der Verordnung (EWG) Nr. 2309/93
zugelassenen Human- oder Tierarzneimitteln festgestellt
werden |
| Dokumentenart: | EudraLex |
