Information adds transparency to the conduct of studies. You can find valuable information anytime in our Study and Registry Portals. They are available to all our partners participating in a project, can be reached online and contain comprehensive information about our studies.
The new Registry Portal is the entry hubfor our tumour 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. With a single set-up you gain access via the platform and are able to document directly. As a consequence the count of participating centres expands from circa 150 to up to 500 centres.