Guideline on good pharmacovigilance practices (GVP) - Module VI – Collection, management and submission of reports of suspecte
![Eu2P Short Course: GVP Module VI - Collection, management and submission of reports of suspected ADR to Medicinal Products Eu2P Short Course: GVP Module VI - Collection, management and submission of reports of suspected ADR to Medicinal Products](https://www.eu2p.org/images/shortcourses/D3SC0019_GVP-Module_VI_Suspected-ADR.jpg)
Eu2P Short Course: GVP Module VI - Collection, management and submission of reports of suspected ADR to Medicinal Products
EMA Guideline on good pharmacovigilance practices (GVP) 4 Module VI – Management and reporting of adverse reactions to medicinal 5 products
Guideline on good pharmacovigilance practices (GVP) - Module VI – Management and reporting of adverse reactions to medicinal p
![Revision 2 of EU Module VI of Guidelines on Good Pharmacovigilance Practices (GVP) - PharSafer® - Specialists in Global Clinical and Post Marketing Drug Safety Revision 2 of EU Module VI of Guidelines on Good Pharmacovigilance Practices (GVP) - PharSafer® - Specialists in Global Clinical and Post Marketing Drug Safety](https://www.pharsafer.com/wp-content/uploads/2017/07/Checking-Facts.jpg)