Webinar: Pharmacovigilance Inspections/Audits & the Role of the QPPV
Important: Registration Deadline is 12 noon on 18 August 2020. All times mentioned are CEST.
Background
What are the tasks and responsibilities of the Qualified Person for Pharmacovigilance (QPPV)? How to implement the requirements in practice - correct and inspection-ready? What is the best way to fulfil the requirement to conduct audits and pharmacovigilance inspections?
This webinar will answer these and other questions and show risk-based approaches on how to deal with the increasing number of audits - e.g. by focusing on audits particularly in critical areas. In this way, time and resources can be saved.
Target Group
Technical Requirements
For our webinars, we use Cisco WebEx, one of the leading suppliers of online meetings.
At http://www.webex.com/test-meeting.html you can check if your system meets the necessary requirements for the participation at a WebEx meeting and at the same time install the necessary plug-in. Please just enter your name and email address for the test. If the installation is not possible because of your rights for the computer system, please contact your IT department. WebEx is a standard nowadays and the necessary installation is fast and easy.
Programme
- Role of the QPPV
- Responsibilities of the QPPV
- Review of the PV system / regular audits
- Audits in an international environment:
- Planning
- Preparation
- Execution
- Follow-up of pharmacovigilance inspections: Post-inspection actions and CAPA management
- Remote audits, joint Audits
| ECA-Member*: | € 199,- |
| Non ECA Member*: | € 249,- |
(All prices excl. VAT). Important notes on sales tax.
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Please contact us:
Tel.: +49 6221 8444-0
E-Mail: info@gmp-compliance.org
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