This BASG discussion will highlight current and future developments relating to the regulatory environment for drug authorisation and life cycle management.
Contents
- PLM Portal (eAF New)
- eCTDv4
- ISO IDMP, SPOR
- Further topics by relevance
Target audience
- Regulatory and technical staff in regulatory affairs departments
- Staff at consulting firms in the pharmaceutical industry
Language
German
Registration information
Please register by 10 June 2026 at the latest.
This event will be held as a hybrid event (participation is possible either online or in person).
Technical Director
DI Georg Neuwirther
Head of IT AGES Medical Market Surveillance
Division, AGES GmbH
Mag. Dr Peter Platzer
Institute for Authorisation & Life Cycle Management Medical
Market Surveillance Division, AGES GmbH