Midterm recruitment report
(si apre in una nuova finestra)
Deliverable will include an overview of recruited subjects by study site, potential recruiting problems and, if applicable, a detailed description of implemented and planned measures to compensate delays in the study subject recruitment.
First study subject approvals package
(si apre in una nuova finestra)
Final version of study protocol as approved by first regulator / ethics committee(s) with its registration number. This deliverable will put together all the ethics documents considered for use of clinical samples.
DMP
(si apre in una nuova finestra)
The DMP describes the data management life cycle for the data to be collected, processed and/or generated. As part of making research data findable, accessible, interoperable and re-usable (FAIR), the DMP will include information on, the handling of research data during & after the end of the project, what data will be collected, processed and/or generated, which methodology & standards will be applied, whether data will be shared/made open access, and how data will be curated & preserved.
Report on status of posting results
(si apre in una nuova finestra)
Report on the status of posting results in the study registry/ies (including timelines when final posting of results is scheduled after end of funding period). To be scheduled for the time of expected results posting or for the last months of the project, whichever comes earlier.