FORUM INSTITUT
FORUM · Institut für Management GmbH
Vangerowstraße 18
69115 Heidelberg
Email: service@forum-institut.de
Phone: +49 6221 500-500
Fax: +49 6221 500-505
Online training Pharmacovigilance
Pharmacovigilance in Europe - Introductory webcast series
2019-12-09 2019-12-09 Online Online

Pharmacovigilance in Europe - Introductory webcast series

3 Packages - 12 Webcasts

Do you need to be well versed in European pharmacovigilance for your daily work? Then we would like to invite you to join this webcast series. You can choose between three different packages according to your level of expertise and requirements.
Topics
  • Package I: Drug adverse reactions
  • Sources and reporting timelines, Signal management and PSURs
  • Package II: Risk management
  • RMP, Risk management system, PRAC and risk management in Europe
  • Package III: Pharmacovigilance system
  • PSMF, Quality management, compliance, inspection and audit readiness

Aims and objectives

This webcast series imparts broad and practical knowledge about all the essentials of European pharmacovigilance in four, eight or 12 live webcasts.
You will acquire the required tools for your daily work in drug safety and meet our experts in a virtual conference room. Each meeting will be a two-hour live webcast, delivering the information with supporting slides (also available for download). Your questions will be addressed directly via the chat function coordinated by the meeting's chair.
Who should attend
This introductory webcast series will be of benefit to all those working in pharmacovigilance or in related departments requiring essential European drug safety expertise. Basic pharmaceutical knowledge is recommended but not a prerequisite.
Your speakers
Dr. Tanja Peters
Boehringer Ingelheim International GmbH, Germany

Dr. Christiane Josupeit
PharmaLex GmbH, Friedrichsdorf, Germany

Dr. Ulrich Vogel
Boehringer Ingelheim International GmbH, Ingelheim, Germany

Dr. Michael Forstner-Dambenois
PrimeVigilance Limited, Swiss

Sven Schirp
Boehringer Ingelheim Pharma GmbH & Co. KG, Germany

Dr Angela van der Salm
DADA Consultancy, Nijmegen, The Netherlands

Dr. Christian M. Moers
Sträter Lawyers, Bonn, Germany

Heike von Treichel
Senior Expert Pharmacovigilance, Darmstadt, Germany

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IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards.

An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2017 - 09.2018) produced a result of 1.6 (based on a school grading system of 1-6).

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