49 results
Keyword azacitidine Remove keyword
Responsible body
COMP Remove COMP filter
PDCO Remove PDCO filter
PRAC Remove PRAC filter
CHMP Remove CHMP filter
Type of content
Events Remove Events filter
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Committee for Medicinal Products for Human Use (CHMP): 14-17 September 2020
Virtual meeting, from 14/09/2020 to 17/09/2020, Last updated: 14/09/2020 -
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Committee for Medicinal Products for Human Use (CHMP): 9-12 November 2020 (updated)
Virtual meeting, from 09/11/2020 to 12/11/2020, Last updated: 07/01/2021 -
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Committee for Orphan Medicinal Products (COMP): 19-21 June 2018
European Medicines Agency, London, UK, from 19/06/2018 to 21/06/2018, Last updated: 17/08/2018 -
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Paediatric Committee (PDCO): 9-11 December 2015
European Medicines Agency, London, UK, from 09/12/2015 to 11/12/2015, Last updated: 09/02/2016 -
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Committee for Orphan Medicinal Products (COMP): 6-8 October 2015
European Medicines Agency, London, UK, from 06/10/2015 to 08/10/2015, Last updated: 27/09/201316 2.1.11. Azacitidine - EMA/OD/098/15 … -
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Committee for Orphan Medicinal Products (COMP): 11-13 September 2018
European Medicines Agency, London, UK, from 11/09/2018 to 13/09/2018, Last updated: 06/12/2018 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 26-29 November 2012
European Medicines Agency, London, UK, from 26/11/2012 to 29/11/2012, Last updated: 26/11/2012 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 1-4 December 2014
European Medicines Agency, London, UK, from 01/12/2014 to 04/12/2014, Last updated: 13/08/2013 -
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Committee for Orphan Medicinal Products (COMP): 10-11 April 2017
European Medicines Agency, London, UK, from 10/04/2017 to 11/04/2017, Last updated: 19/06/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 2-5 December 2013
European Medicines Agency, London, UK, from 02/12/2013 to 05/12/2013, Last updated: 02/07/2012 -
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Committee for Orphan Medicinal Products (COMP): 10-12 November 2015
European Medicines Agency, London, UK, from 10/11/2015 to 12/11/2015, Last updated: 27/09/2013 -
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Workshop on site and histology - Independent indications in oncology
European Medicines Agency, London, UK, from 14/12/2017 to 15/12/2017, Last updated: 07/02/2018 -
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Committee for Orphan Medicinal Products (COMP): 22-24 May 2018
European Medicines Agency, London, UK, from 22/05/2018 to 24/05/2018, Last updated: 17/08/2018 -
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Committee for Orphan Medicinal Products (COMP): 8-10 December 2015
European Medicines Agency, London, UK, from 08/12/2015 to 10/12/2015, Last updated: 27/09/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 11-14 January 2016
European Medicines Agency, London, UK, from 11/01/2016 to 14/01/2016, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 May 2013
European Medicines Agency, London, UK, from 13/05/2013 to 16/05/2013, Last updated: 02/07/2012 -
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Committee for Medicinal Products for Human Use (CHMP): 21-24 September 2015
European Medicines Agency, London, UK, from 21/09/2015 to 24/09/2015, Last updated: 03/01/2014 -
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Committee for Orphan Medicinal Products (COMP): 11-13 July 2017
European Medicines Agency, London, UK, from 11/07/2017 to 13/07/2017, Last updated: 19/06/2014 -
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Committee for Orphan Medicinal Products (COMP): 17-19 January 2017
European Medicines Agency, London, UK, from 17/01/2017 to 19/01/2017, Last updated: 18/06/2014 -
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Committee for Orphan Medicinal Products (COMP): 19-21 January 2016
European Medicines Agency, London, UK, from 19/01/2016 to 21/01/2016, Last updated: 17/06/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 4-7 March 2013
European Medicines Agency, London, UK, from 04/03/2013 to 07/03/2013, Last updated: 02/06/2012 -
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Committee for Orphan Medicinal Products (COMP): 17-19 July 2018
European Medicines Agency, London, UK, from 17/07/2018 to 19/07/2018, Last updated: 19/06/2014 -
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Paediatric Committee (PDCO): 12-14 August 2015
European Medicines Agency, London, UK, from 12/08/2015 to 14/08/2015, Last updated: 19/02/2013 -
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Committee for Orphan Medicinal Products (COMP): 17-19 April 2018
European Medicines Agency, London, UK, from 17/04/2018 to 19/04/2018, Last updated: 16/04/2018 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 April 2015
European Medicines Agency, London, UK, from 07/04/2015 to 10/04/2015, Last updated: 20/05/2015