Personal tools

Sponsorname

Your company could advertise here

www.fla-consulting.eu

Reference:EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) -

From GxPlex

Revision as of 13:49, 16 July 2026 by Gxplex admin (talk | contribs) (1 revision imported)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to: navigation, search



Document information
Reference EU GVP: Module VIII

EMA/813938/2011 Rev. 3 (2017)

Validity area EU
Scope(s) NIS
Document name GVP: Module VIII

EMA/813938/2011

Version / Revision Rev. 3 (2017)
Status Current
Document type Official guideline
Language(s) EN
Description Guideline on good pharmacovigilance practices (GVP)

Module VIII – Post-authorisation safety studies (Rev 3)

Official source Official link
Restricted access No
Submitted by Florian Adragna
Contributors


Reference Details
Module Module 2 — Unit 2.1.3
Scope NIS
Document part -
Language EN
Original entry by Florian Adragna
Contributors
Tags Post-authorisation safety study, Protocol, Requirements

Content

[...] VIII.B.3. Study protocol [...] VIII.B.3.1. Format and content of the study protocol [...]