Information ensures transparency in the conduct of studies. Valuable information can be found in our study and registry portals, which are available to all partners participating in a project, can be accessed online and contain comprehensive information about our studies.
The new Registry Portal is the entry hub for our tumor registries and registry platforms. Our new PAN registry concept makes the difference: participation in one registry enables study sites to recruit patients for all other entities as well. A single set-up allows access via the platform and direct documentation. Thus, the number of participating centers increases from around 150 to up to 500.