COM(2010)3 - Application of Directive 2002/98/EC setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components

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Contents

  1. Key information
  2. Key dates
  3. Related information
  4. Full version
  5. EU Monitor

1.

Key information

official title

Communication from the Commission to the Council, the European Parliament, the European Economic and Social Committee and the Committee of the Regions on the application of Directive 2002/98/EC 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
 
Legal instrument Communication
reference by COM-number51 COM(2010)3 EN
Additional COM-numbers COM(2010)3
CELEX number54 52010DC0003

2.

Key dates

Document 19-01-2010
Online publication 19-01-2010

3.

Related information

 

4.

Full version

This page is also available in a full version containing the latest state of affairs, the summary of the European Parliament Legislative Observatory, the legal context, other dossiers related to the dossier at hand, the stakeholders involved (e.g. European Commission directorates-general, European Parliament committees, Council configurations and even individual EU Commissioners and Members of the European Parliament) and finally documents of the European Parliament, the Council of Ministers and the European Commission.

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5.

EU Monitor

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  • 1. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 2. 
    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 (OJ L 91, 30.3.2004, p. 25).

     
  • 3. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 4. 
    Commission Directive 2005/62/EC of 30 September 2005 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards Community standards and specifications relating to a quality system for blood establishments (OJ L 256, 1.10.2005, p. 41).

     
  • 5. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 6. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 7. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 8. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 9. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 10. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 11. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 12. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 13. 
    According to Article 3(g) of Directive 2002/98/EC,
     
  • 14. 
    According to Article 3 (h) of Directive 2002/98/EC,
     
  • 15. 
    ec.europa.eu/health/ph_threats/human_substance

     
  • 16. 
    Testing for presence of Hepatitis B antibodies.

     
  • 17. 
    Nucleic acid amplification technique for testing Hepatitis B.

     
  • 18. 
    Nucleic acid amplification technique for testing Hepatitis C.

     
  • 19. 
    Testing for presence of HIV antigens.

     
  • 20. 
    Nucleic acid amplification technique for testing HIV1.

     
  • 21. 
    Bacteria generally acquired by close sexual contact giving rise to congenital syphilis.

     
  • 22. 
    Human T-lymphotropic virus.

     
  • 23. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 24. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 25. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 26. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 27. 
    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 (OJ L 91, 30.3.2004, p. 25).

     
  • 28. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 29. 
    Commission Directive 2005/62/EC of 30 September 2005 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards Community standards and specifications relating to a quality system for blood establishments (OJ L 256, 1.10.2005, p. 41).

     
  • 30. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 31. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 32. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 33. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 34. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 35. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 36. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 37. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 38. 
    According to Article 3(g) of Directive 2002/98/EC,
     
  • 39. 
    According to Article 3 (h) of Directive 2002/98/EC,
     
  • 40. 
    ec.europa.eu/health/ph_threats/human_substance

     
  • 41. 
    Testing for presence of Hepatitis B antibodies.

     
  • 42. 
    Nucleic acid amplification technique for testing Hepatitis B.

     
  • 43. 
    Nucleic acid amplification technique for testing Hepatitis C.

     
  • 44. 
    Testing for presence of HIV antigens.

     
  • 45. 
    Nucleic acid amplification technique for testing HIV1.

     
  • 46. 
    Bacteria generally acquired by close sexual contact giving rise to congenital syphilis.

     
  • 47. 
    Human T-lymphotropic virus.

     
  • 48. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 49. 
    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 blood and blood components (OJ L 33, 8.2.2003, p. 30).

     
  • 50. 
    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 (OJ L 256, 1.10.2005, p. 32).

     
  • 51. 
    De Europese Commissie kent nummers toe aan officiële documenten van de Europese Unie. De Commissie maakt onderscheid in een aantal typen documenten door middel van het toekennen van verschillende nummerseries. Het onderscheid is gebaseerd op het soort document en/of de instelling van de Unie van wie het document afkomstig is.
     
  • 52. 
    De Raad van de Europese Unie kent aan wetgevingsdossiers een uniek toe. Dit nummer bestaat uit een vijfcijferig volgnummer gevolgd door een schuine streep met de laatste twee cijfers van het jaartal, bijvoorbeeld 12345/00 - een document met nummer 12345 uit het jaar 2000.
     
  • 53. 
    Het interinstitutionele nummer is een nummerreeks die binnen de Europese Unie toegekend wordt aan voorstellen voor regelgeving van de Europese Commissie.
    Binnen de Europese Unie worden nog een aantal andere nummerseries gebruikt. Iedere instelling heeft één of meerdere sets documenten met ieder een eigen nummering. Die reeksen komen niet overeen met elkaar of het interinstitutioneel nummer.
     
  • 54. 
    Deze databank van de Europese Unie biedt de mogelijkheid de actuele werkzaamheden (workflow) van de Europese instellingen (Europees Parlement, Raad, ESC, Comité van de Regio's, Europese Centrale Bank, Hof van Justitie enz.) te volgen. EURlex volgt alle voorstellen (zoals wetgevende en begrotingsdossiers) en mededelingen van de Commissie, vanaf het moment dat ze aan de Raad of het Europees Parlement worden voorgelegd.
     
  • 55. 
    Als dag van bekendmaking van een Europees besluit geldt de dag waarop het besluit in het Publicatieblad wordt bekendgemaakt, en daardoor in alle officiële talen van de Europese Unie bij het Publicatiebureau beschikbaar is.