Is it even possible to implement application-related data collection?
Legislators have opened the door to application-related data collection for the benefit assessment of new drugs. This presents an opportunity for real-world evidence. However, the requirements under discussion are demanding. Can clinical registries in Germany currently meet these requirements? And could these requirements even be achieved with a reasonable amount of effort? A recent study takes stock of the situation.
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First publication date: 02.04.2020
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Literature
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- Issue: Issue 02/2020 Publication Date: 02.04.2020 All issues as PDF Subscribe to print magazine Order single issue Open Access