12 results
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Human medicine European public assessment report (EPAR): Akynzeo (updated)
netupitant, palonosetron hydrochloride, Vomiting; Neoplasms; Nausea; Cancer
Date of authorisation: 27/05/2015, Revision: 16, Authorised, Last updated: 08/09/2023 -
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Human medicine European public assessment report (EPAR): Zinbryta
daclizumab, Multiple Sclerosis
Date of authorisation: 01/07/2016,
, Revision: 8, Withdrawn, Last updated: 28/06/2018
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Referral: Sandimmun and associated names
ciclosporin, Article 30 referrals
Status: European Commission final decision, opinion/position date: 27/06/2013, EC decision date: 31/10/2013, Last updated: 20/12/2013 -
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Referral: Sandimmun Neoral and associated names
ciclosporin, Article 30 referrals
Status: European Commission final decision, opinion/position date: 27/06/2013, EC decision date: 31/10/2013, Last updated: 20/12/2013 -
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Referral: Zinbryta
daclizumab, associated names: Zinbryta, Article 20 procedures
Status: European Commission final decision, opinion/position date: 09/11/2017, EC decision date: 08/01/2018, Last updated: 12/01/2018 -
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Public data from Article 57 database
Last updated: 30/06/2023 -
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Consultation meeting with stakeholders: Request from the European Commission for advice on the impact on public and animal health of the use of antibiotics in animals
European Medicines Agency, London, UK, 28/02/2014, Last updated: 03/04/2014 -
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Workshop on clinical development and scientific advice in ophthalmology
European Medicines Agency, London, from 27/10/2011 to 28/10/2011, Last updated: 04/07/2011 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 April 2013
European Medicines Agency, London, UK, from 08/04/2013 to 11/04/2013, Last updated: 02/06/2012 -
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Guidance documents
Last updated: 19/07/2022 -
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PRAC: Committee agendas, minutes and meeting highlights report archive 2012-2013
Last updated: 01/01/2015 -
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PRAC: meeting archive 2012-2014
Last updated: 13/05/2016