Leistungen
AEMPS approval to conduct the 3 phase I studies in healthy volunteers SAD MAD and FEThis package will include a final version of study protocol as approved by regulatory agencyiesethics committees a study registration number in EudraCT European Union Drug Regulating Authorities Clinical Trials Database and copies of opinions andor authorization from Institutional Data Protection Officer and National Data Protection Authority as appropriate
Intermediary report on dissemination and communication activitiesReport summarizing all the dissemination and communication activities educational days press conferences oopen public onferences articles or press releases performed during the first half part of the ICOD project
Report on Scientific meetings participationsReport of the participation to international scientific meetings with posters orand talks from the researchers involved in the project such as the Annual Meeting of the American Society for Neuroscience Meeting SfN and most importantly the Trisomy21 Research Society T21RS International Research Conference IRC
ICOD Project Management handbookHandbook summarizing the operating rules of the project management office PMO
Availability of the project website online with external contribution of EDSA and national DS associations
Corporate identity, video & flyerAvailability of a project logo and a professional corporate identity which will appear on all documents publications and ICOD presentations Flyers will be produced to be hand out at events at which the ICOD project will participate Youtube channel with videos conveyed on social networking sites for young people
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