In this BASG discussion, we will provide you with information on the regulatory and pharmaceutical quality aspects of variations.
Contents
- Regulatory feedback – case studies following the revision of variation regulations and guidelines
- “Drug-Device Combinations in Variations”
- “ICH Q12 Tools – PACMP and PLCM”
You can find the detailed programme here.
Target audience
- Regulatory staff in regulatory affairs departments
- Staff at consulting firms in the pharmaceutical industry
Language
German
Registration information
Please register by 25 November 2026 at the latest.
This event will be held entirely online.
Technical Director
Mag. Dr Peter Platzer
Institute for Regulatory Affairs & Life Cycle Management Medical
Market Surveillance Division, AGES GmbH