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FDA - Pharmacovigilance Requirements
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Providing Submissions in Electronic Format— Postmarketing Safety Reports Guidance for IndustryBy VigiServe Admin0 Replies · 250 ViewsLast post: 3 years ago · VigiServe Admin
FDA VAERS - Vaccine Adverse Event Reporting SystemBy VigiServe Admin4 Replies · 1,109 ViewsLast post: 3 years ago · VigiServe Admin
PADERs and Aggregate Reports in USBy VigiServe Admin1 Reply · 444 ViewsLast post: 4 years ago · VigiServe Admin
Clinical Safety in the United StatesBy VigiServe Admin0 Replies · 205 ViewsLast post: 4 years ago · VigiServe Admin
Pharmacovigilance Requirements in US - CFR 314.80By VigiServe Admin0 Replies · 286 ViewsLast post: 4 years ago · VigiServe Admin