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Pharmacovigilance Requirements in the European Union / European Economic Area
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Exploitant requiremements in FranceBy VigiServe Admin1 Reply · 271 ViewsLast post: 2 years ago · VigiServe Admin
Important Medical Events (IME)By VigiServe Admin1 Reply · 346 ViewsLast post: 3 years ago · VigiServe Admin
Designated Medical Event (DME) listBy VigiServe Admin0 Replies · 1,534 ViewsLast post: 3 years ago · VigiServe Admin
HMPC - Committee on Herbal Medicinal ProductsBy VigiServe Admin1 Reply · 203 ViewsLast post: 4 years ago · VigiServe Admin
Graduated plan officer (Stufenplanbeauftragter) in GermanyBy VigiServe Admin2 Replies · 485 ViewsLast post: 4 years ago · VigiServe Admin
PRAC - Pharmacovigilance Risk Assessment CommitteeBy VigiServe Admin1 Reply · 191 ViewsLast post: 4 years ago · VigiServe Admin
Submitting RMP in the EU/EEABy VigiServe Admin3 Replies · 211 ViewsLast post: 4 years ago · VigiServe Admin
Which products qualify for Central Authorisation in the EU/EEA?By VigiServe Admin0 Replies · 157 ViewsLast post: 4 years ago · VigiServe Admin
Pharmacovigilance System Master FileBy VigiServe Admin2 Replies · 371 ViewsLast post: 4 years ago · VigiServe Admin
QPPV Requirements in EU/EEABy VigiServe Admin0 Replies · 618 ViewsLast post: 4 years ago · VigiServe Admin
Summary of Pharmacovigilance System (SPS)By VigiServe Admin0 Replies · 323 ViewsLast post: 4 years ago · VigiServe Admin