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Pharmacovigilance Requirements in the European Union / European Economic Area
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Exploitant requiremements in FranceBy VigiServe Admin1 Reply · 328 ViewsLast post: 3 years ago · VigiServe Admin
Important Medical Events (IME)By VigiServe Admin1 Reply · 402 ViewsLast post: 4 years ago · VigiServe Admin
Designated Medical Event (DME) listBy VigiServe Admin0 Replies · 1,737 ViewsLast post: 4 years ago · VigiServe Admin
HMPC - Committee on Herbal Medicinal ProductsBy VigiServe Admin1 Reply · 242 ViewsLast post: 4 years ago · VigiServe Admin
Graduated plan officer (Stufenplanbeauftragter) in GermanyBy VigiServe Admin2 Replies · 602 ViewsLast post: 4 years ago · VigiServe Admin
PRAC - Pharmacovigilance Risk Assessment CommitteeBy VigiServe Admin1 Reply · 232 ViewsLast post: 4 years ago · VigiServe Admin
Submitting RMP in the EU/EEABy VigiServe Admin3 Replies · 264 ViewsLast post: 4 years ago · VigiServe Admin
Which products qualify for Central Authorisation in the EU/EEA?By VigiServe Admin0 Replies · 191 ViewsLast post: 4 years ago · VigiServe Admin
Pharmacovigilance System Master FileBy VigiServe Admin2 Replies · 488 ViewsLast post: 4 years ago · VigiServe Admin
QPPV Requirements in EU/EEABy VigiServe Admin0 Replies · 751 ViewsLast post: 4 years ago · VigiServe Admin
Summary of Pharmacovigilance System (SPS)By VigiServe Admin0 Replies · 463 ViewsLast post: 4 years ago · VigiServe Admin