In this BASG discussion, we will provide you with information on how to correctly draft product information and patient information leaflets for medicinal products. The agenda also includes topics such as labelling and mock-ups, as well as key aspects of the name verification process for medicinal products.
Contents
- Correct design of prescribing information and patient information leaflets
- Correct design of labelling and mock-ups
- Aspects of the name review process for medicinal products
- Prescription-only
- Exchange of experiences and discussion
You can find the detailed programme here.
Target audience
- Regulatory staff in regulatory affairs departments and
- staff at consulting firms in the pharmaceutical industry
Language
German
Registration information
Please register by 11 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