The content of this BASG discussion is the assessment of the quality of human medicinal products. Current quality-related issues will be discussed.
Contents
- How to use a CEP
- Quality requirements for clinical trial products
- Quality documentation for medicinal products when used with a medical device
- News on a "Hot Topic 2024" (topic to be announced)
Target group
- Regulatory and technical employees of authorisation departments
- Employees of consulting companies in the pharmaceutical industry
Language
Presentation language German, slides in English
Registration information
Please register at by 16 October 2024 at the latest.
This event will be held as an online-only event .
Subject leader and lecturer
Dr Peter Platzer
Head of Institute Regulatory Affairs & Life Cycle Management
Business Unit Medical Market Surveillance, AGES GmbH