At this BASG meeting, we will inform you about current and future developments in the field of clinical trials of medicinal products.
Contents
- Regulation (EU) No 536/2014 on clinical trials and the EU Biotech Act
- Developments in the Clinical Trial Information System (CTIS)
- European initiatives and information from the European working groups (CTCG, CTAG, GCP IWG)
- National specifics, best practices and case studies
- Interfaces with other legal matters such as medical devices or cells/tissues
- Exchange of experiences and discussion
The detailed programme can be found [url_begin|programme|link|here|url_end].
Target
- Employees of regulatory affairs departments in the pharmaceutical industry
- Employees of contract research organisations (CROs) and self-employed persons
- Employees of clinical trial coordination centres (KKS)
- Academic researchers
Language
German
Registration
- Please register by 20 May 2026 at the latest.
- This BASG discussion will take place exclusively in person at the Vienna General Hospital.
- Registration is located on level 7.
Technical management
Dr Stefan Strasser
Clinical Trials Department, Institute for Monitoring
Medical Market Surveillance, AGES GmbH
Training information
Four DFP points have been approved for this event.
In cooperation with
GPMed – Austrian Society for Pharmaceutical Medicine