2026-03-05 2026-03-05 , online online, 1,790 € zzgl. MwSt. Pharmacovigilance Auditing

Do you want to independently plan and conduct pharmacovigilance audits? Then take this opportunity to become an "Auditor for Good Pharmacovigilance Practices". Secure your place on our compact, interactive online course. Book now!

Themen
  • Qualifications and responsibilities according to GVP Module IV
  • Conducting effective interviews
  • Auditing of PV documents, contracts, and SDEAs
  • Expectations of an auditor and inspector
  • Risk-based audit strategy - planning, scheduling, and execution


Who should attend
This course will be conducted in English.

This online course is aimed at professionals and managers in the pharmaceutical industry who aspire to, or have recently achieved, the role of GVP auditor and wish to plan and conduct pharmacovigilance audits independently and confidently in the future.

Work experience in pharmacovigilance of more than three years is recommended for this course.
Ziel der Veranstaltung
In just 1.5 days, our compact, interactive training programme will fully prepare you to conduct sound Good Pharmacovigilance Practice (GVP) audits.

After covering the basics of EU regulation, the first day focuses on the key tasks of the auditor: Conducting interviews with PV responsibilities or managers and reviewing various PV documents.
Day 2 begins with a holistic view of all the areas that need to be assessed in a PV audit. Different strategies will be discussed depending on who is auditing whom and the risk-based approach to PV audits will be trained.

During the training our qualified experts will answer many other additional questions such as:
  • Where can I find supporting material such as checklists, templates, and questionnaires?
  • What are the expectations of an inspector regarding the planning, execution, and documentation of an audit?
Teilnehmerkreis

Take advantage of this compact online training course and conduct future pharmacovigilance audits safely, independently and successfully! The two workshops included will help you consolidate what you have learned and put it into practice.

After the seminar, you will be able to...

  • accompany and conduct pharmacovigilance audits according to the latest regulations.
  • conduct targeted and effective interviews.
  • understand pharmacovigilance contracts and key pharmacovigilance documents in detail.
  • develop risk-based audit strategies and audit plans.

Online Course - Pharmacovigilance Auditing

Pharmacovigilance Auditing

Planning and conducting GVP Audits

Benefits
  • Compact training for new PV auditors
  • Professional speakers from Big Pharma and consulting
  • Interactive format with workshops and test
  • Officially certified to the ISO 9001 and ISO 21001 standards

Webcode 26102051

Jetzt buchen

JETZT Buchen

Alles auf einen Blick

Termin

12 - 13/10/2026

12 - 13/10/2026

Zeitraum

Day 1: 09:00-17:00 CE(S)T
Day 2: 09:00-13:00 CE(S)T
You may dial in 30 min before the course starts

Day 1: 09:00-17:00 CE(S)T
Day 2: 09:00-13:00 CE(S)T
You may dial in 30 min before the course starts
Veranstaltungsort

online

online

Downloads
Gebühr
Your contact

Nadja Wolff
Conference Manager

+49 6221 500-696
n.wolff@forum-institut.de

Details

Do you want to independently plan and conduct pharmacovigilance audits? Then take this opportunity to become an "Auditor for Good Pharmacovigilance Practices". Secure your place on our compact, interactive online course. Book now!

Themen

  • Qualifications and responsibilities according to GVP Module IV
  • Conducting effective interviews
  • Auditing of PV documents, contracts, and SDEAs
  • Expectations of an auditor and inspector
  • Risk-based audit strategy - planning, scheduling, and execution


Who should attend
This course will be conducted in English.

This online course is aimed at professionals and managers in the pharmaceutical industry who aspire to, or have recently achieved, the role of GVP auditor and wish to plan and conduct pharmacovigilance audits independently and confidently in the future.

Work experience in pharmacovigilance of more than three years is recommended for this course.

Ziel der Veranstaltung

In just 1.5 days, our compact, interactive training programme will fully prepare you to conduct sound Good Pharmacovigilance Practice (GVP) audits.

After covering the basics of EU regulation, the first day focuses on the key tasks of the auditor: Conducting interviews with PV responsibilities or managers and reviewing various PV documents.
Day 2 begins with a holistic view of all the areas that need to be assessed in a PV audit. Different strategies will be discussed depending on who is auditing whom and the risk-based approach to PV audits will be trained.

During the training our qualified experts will answer many other additional questions such as:

  • Where can I find supporting material such as checklists, templates, and questionnaires?
  • What are the expectations of an inspector regarding the planning, execution, and documentation of an audit?

Teilnehmerkreis

Take advantage of this compact online training course and conduct future pharmacovigilance audits safely, independently and successfully! The two workshops included will help you consolidate what you have learned and put it into practice.

After the seminar, you will be able to...

  • accompany and conduct pharmacovigilance audits according to the latest regulations.
  • conduct targeted and effective interviews.
  • understand pharmacovigilance contracts and key pharmacovigilance documents in detail.
  • develop risk-based audit strategies and audit plans.