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Keyword Binocrit Remove keyword
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Human medicine European public assessment report (EPAR): Binocrit
epoetin alfa, Anemia, Kidney Failure, Chronic
Date of authorisation: 28/08/2007,
, Revision: 20, Authorised, Last updated: 31/10/2019
Binocrit Anemia Kidney Failure … Binocrit … Binocrit, INN-epoetin alfa European … -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 July 2018
CHMP, Last updated: 27/07/2018Abseamed, Binocrit … -
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Press release: EMEA recommends a new warning for epoetins for their use in cancer patients
CHMP, Last updated: 26/06/2008epoetin zeta) and Abseamed, Binocrit and Epoetin Alfa Hexal (epoetin … epoetin zeta) and Abseamed, Binocrit and Epoetin Alfa Hexal (epoetin … -
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Human medicine European public assessment report (EPAR): Epoetin Alfa Hexal
epoetin alfa, Anemia, Kidney Failure, Chronic, Cancer
Date of authorisation: 27/08/2007,, Revision: 22, Authorised, Last updated: 09/10/2019
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Committee for Medicinal Products for Human Use (CHMP): 25-29 January 2021 (updated)
Virtual meeting, from 25/01/2021 to 29/01/2021, Last updated: 04/03/2021 -
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CHMP: Agendas, minutes and highlights
Last updated: 29/01/2021 -
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PRAC: Agendas, minutes and highlights (updated)
Last updated: 16/02/2021 -
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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 Medicinal Products for Human Use (CHMP): 23-26 July 2018
European Medicines Agency, London, UK, from 23/07/2018 to 26/07/2018, Last updated: 06/01/2014 -
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Committee for Medicinal Products for Human Use (CHMP): 17-20 September 2018
European Medicines Agency, London, UK, from 17/09/2018 to 20/09/2018, Last updated: 31/10/2018 -
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Gulf Cooperation Council (GCC) Biosimilar Medicinal Products Workshop
Riyadh, Saudi Arabia, from 19/04/2011 to 20/04/2011, Last updated: 23/06/2011 -
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Committee for Medicinal Products for Human Use (CHMP): 15-18 May 2017
European Medicines Agency, London, UK, from 15/05/2017 to 18/05/2017, Last updated: 06/01/2014 -
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Download medicine data
Last updated: 29/04/2020 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 February 2015
European Medicines Agency, London, UK, from 09/02/2015 to 12/02/2015, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 March 2015
European Medicines Agency, London, UK, from 09/03/2015 to 12/03/2015, Last updated: 13/03/2014 -
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Committee for Medicinal Products for Human Use (CHMP): 10-13 October 2016
European Medicines Agency, London, UK, from 10/10/2016 to 13/10/2016, Last updated: 06/01/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 July 2014
European Medicines Agency, London, UK, from 07/07/2014 to 10/07/2014, Last updated: 13/08/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 February 2017
European Medicines Agency, London, UK, from 06/02/2017 to 09/02/2017, Last updated: 13/03/2014 -
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Committee for Medicinal Products for Human Use (CHMP): 6-9 November 2017
European Medicines Agency, London, UK, from 06/11/2017 to 09/11/2017, Last updated: 06/01/2014 -
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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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Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 February 2016
European Medicines Agency, London, UK, from 08/02/2016 to 11/02/2016, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 3-6 July 2017
European Medicines Agency, London, UK, from 03/07/2017 to 06/07/2017, Last updated: 13/03/2014 -
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PRAC: meeting archive 2012-2013
Last updated: 13/05/2016 -
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EMEA workshop on Monoclonal Antibodies
London, 02/07/2009, Last updated: 01/07/2009 -
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PRAC: Committee agendas, minutes and meeting highlights report archive 2012-2013
Last updated: 01/01/2015