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The MDR harvests metadata on data objects from a variety of sources within clinical research (e.g. trial registries, data repositories) and brings that together in a single searchable portal. The metadata is concerned with discoverability, access and provenance of the data objects (which because the data may be sensitive will often be available under a controlled access regime). At the moment (01/2021) the MDR obtains study data from: Clinical Trials.gov (CTG), The European Clinical Trials Registry (EUCTR), ISRCTN, The WHO ICTRP
The opendata.swiss portal is a joint project of the Confederation, cantons, communes and other organizations with a mandate from the state. It makes open government data available to the general public in a central catalogue. opendata.swiss is operated by the Federal Statistical Office.