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Are you feeling constrained by the complexities of the pharmacovigilance regulations in the EU?

This e-book will provide you with key tips to successfully navigate pharmacovigilance for clinical trials in the EU

This guide will:

1
Give you an overview of the EU’s legislations on Pharmacovigilance
2
Illustrate the type of information you should collect and who to report it to
3
Show the “best practice” strategies to follow
GET YOUR FREE E-BOOK HERE
“Pharmacovigilance moves more and more into the focus of regulatory agencies. Existing regulations within the EU become much more complex and it is difficult to navigate through the jungle of directives, regulations and guidelines. 

The requirements and expectations increase and, at the same time, it becomes more important to not lose track of transparency. 

This e-book will help you to determine the most important challenges of Pharmacovigilance and offer a guide through European PV-related legislation.”

Kerstin Fleischer

Head of Pharmacovigilance, Dokumeds

Our e-book will provide you with in-depth information on:

How to reconcile the demands of the EMA and the GDPR

The responsibilities expected of marketing authorisation holders regarding reporting of adverse events

How to process the pharmacovigilance data you capture

The advantages offered by qualified CROs with specific experience in pharmacovigilance

GET YOUR FREE E-BOOK HERE