As part of this BASG discussion, we will inform you about the official procedure for processing quality defect reports for medicinal products and the corresponding legal basis. You will also receive information on the frequency of reports in recent years.
Contents
- Legal basis
- Processing procedure
- Statistics
- Exchange of experience and discussion
Target group
- Employees of the pharmaceutical industry
- Employees of consulting companies in the pharmaceutical industry
Language
German
Registration information
Please registerat by 26 March 2025 at the latest.
This event will be held as a hybrid event (participation online or in person on site possible).
Technical management
DI Dr Sabine Sereinig
Group Quality Defects
Department Enforcement, Distribution Restrictions & Quality Defects
Institute Surveillance
Business Unit Medical Market Surveillance, AGES GmbH