The European Medicines Agency is consulting stakeholders on an amended risk management plan (RMP) template, to be used by medicine developers. The revision of the template is based on the principles described in the updated good pharmacovigilance practices (GVP) module V in the view of getting a focussed risk management system and simplifying the way information is submitted to the regulators.
|Download document||Draft guidance on format of the risk management plan (RMP) in the EU – in integrated format|
|Reference number||EMA/PRAC/613102/2015 Rev.2 accompanying GVP Module|
|Status||draft: consultation open|
|Consultation start date||29/02/2016|
|Consultation end date||31/05/2016|
|Email address for email@example.com|