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EU/EEA
Pharmacovigilance Requirements in the European Union / European Economic Area
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Submitting RMP in the EU/EEABy VigiServe Admin4 Replies · 787 ViewsLast post: 1 year ago · VigiServe Admin
Exploitant requiremements in FranceBy VigiServe Admin1 Reply · 626 ViewsLast post: 4 years ago · VigiServe Admin
Important Medical Events (IME)By VigiServe Admin1 Reply · 872 ViewsLast post: 5 years ago · VigiServe Admin
Designated Medical Event (DME) listBy VigiServe Admin0 Replies · 2,468 ViewsLast post: 5 years ago · VigiServe Admin
HMPC - Committee on Herbal Medicinal ProductsBy VigiServe Admin1 Reply · 388 ViewsLast post: 6 years ago · VigiServe Admin
Graduated plan officer (Stufenplanbeauftragter) in GermanyBy VigiServe Admin2 Replies · 922 ViewsLast post: 6 years ago · VigiServe Admin
PRAC - Pharmacovigilance Risk Assessment CommitteeBy VigiServe Admin1 Reply · 508 ViewsLast post: 6 years ago · VigiServe Admin
Which products qualify for Central Authorisation in the EU/EEA?By VigiServe Admin0 Replies · 286 ViewsLast post: 6 years ago · VigiServe Admin
Pharmacovigilance System Master FileBy VigiServe Admin2 Replies · 3,067 ViewsLast post: 6 years ago · VigiServe Admin
QPPV Requirements in EU/EEABy VigiServe Admin0 Replies · 2,017 ViewsLast post: 6 years ago · VigiServe Admin
Summary of Pharmacovigilance System (SPS)By VigiServe Admin0 Replies · 1,477 ViewsLast post: 6 years ago · VigiServe Admin