This BASG discussion will highlight current and future developments in the regulatory environment of medicinal product authorisation and life cycle management.
Contents
- PLM Portal (eAF New)
- eCTDv4
- ISO IDMP, SPOR
- Further topics according to relevance
Target group
- Regulatory and technical employees in authorisation departments
- Employees of consulting companies in the pharmaceutical industry
Language
German
Registration information
Please registerat by 11 June 2025 at the latest.
This event will be held as an online-only event .
Technical management
DI Georg Neuwirther
Head of IT AGES Medical Market Surveillance
Business Unit Medical Market Surveillance, AGES GmbH
Dr Peter Platzer
Institute for Regulatory Affairs & Life Cycle Management
Medical Market Surveillance Division, AGES GmbH