Directiva 2005/61/CE de la Comisión, de 30 de septiembre de 2005, por la que se aplica la Directiva 2002/98/CE del Parlamento Europeo y del Consejo en lo relativo a los requisitos de trazabilidad y a la notificación de reacciones y efectos adversos graves (1)
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Directiva 2005/61/CE de la Comisión, de 30 de septiembre de 2005, por la que se aplica la Directiva 2002/98/CE del Parlamento Europeo y del Consejo en lo relativo a los requisitos de trazabilidad y a la notificación de reacciones y efectos adversos graves (1)
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Documentos citados
- Commission Directive 2005/61/EC of 30 September 2005 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards traceability requirements and notification of serious adverse reactions and events (Text with EEA relevance)
- Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
- Directive 2002/98/EC of the European Parliament and of the Council of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components and amending Directive 2001/83/EC
- Commission Directive 2004/33/EC of 22 March 2004 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards certain technical requirements for blood and blood components (Text with EEA relevance)
- Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance)
