Good Pharmacovigilance Practices - Further Modules Released for Public Consultation
30/04/2013 - The European Medicines Agency has released further modules/updates of the guildeline on Good Pharmacovigilance Practices (GVP) for public consultation.
· GVP: Product-or population-specific considerations I: Vaccines for prophylaxis against infectious
diseases
· GVP PI – Vaccines for prophylaxis against infectious diseases – Definitions for inclusion in GVP annex I
· Module VII – Periodic safety update reports – Revision 1
Good Pharmacovigilance Practices - Further Two Modules Released for Public Consultation
26/07/2012 - The European Medicines Agency released two further modules of the guideline on Good Pharmacovigilance Practices (GVP) for public consultation.
This consultation process has now closed. The deadline for comments was 21 September 2012.
Good Pharmacovigilance Practices - Further Two Modules Released for Public Consultation
27/06/2012 - The European Medicines Agency released two further modules of the guideline on Good Pharmacovigilance Practices (GVP) for public consultation.
This consultation process has now closed. The deadline for comments was 24 August 2012.
Department of Health Public Consultation
22/06/2012 - The Department of Health initiated a public consultation on the transposition of the EU pharmacovigilance legislation. The views of the public and interested parties were sought on draft regulations transposing EU Directive 2010/84/EU and EU Regulation 1235/2010/EU on pharmacovigilance.
http://www.dohc.ie/consultations/open/pharmacovigilance
This consultation process has now closed. The deadline for comments was 6 July 2012. This legislation was transposed into Irish law in late July 2012.