CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.
Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .
Rezultaty
Guidelines and rules for the coordination, reporting and quality control of the project
Pilot study initiation package - Italy-USG-Young Adults (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Portugal-UC-Young Adults (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Portugal-UEV-Children (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Denmark-DTU-Children (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - The Netherlands-TU/e-Children & Young Adults (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Bulgaria-RCNE-Children (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Germany-DFKI/BIPS-Children & Young adults (odnośnik otworzy się w nowym oknie)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
CDTEC - plan (odnośnik otworzy się w nowym oknie)Comprehensive CDTEC plan with elements of the project identity, targeted events and actions including a mapping of actors to be targeted and a set of KPIs to monitor activities
Detailed DMP describing various data types, datasets, data quality & privacy issues, data management procedures, IT infrastructure and the data governance model
Official release of fully functional OSP based on partner & user feedbacks
HealthyW8 public website (odnośnik otworzy się w nowym oknie)A public project website to disseminate non-confidential project content (reports, publications as part of our open access strategy, etc.) and training & education tools to the target audiences and to house a restricted access area for partners to share information
Publikacje
Autorzy:
Farhad Vahid, Coralie Dessenne, Josep A Tur, Cristina Bouzas, Yvan Devaux, Laurent Malisoux, Margalida Monserrat-Mesquida, Antoni Sureda, Mahesh S Desai, Jonathan D Turner, Elsa Lamy, Maria Perez-Jimenez, Gitte Ravn-Haren, Rikke Andersen, Sarah Forberger, Rajini Nagrani, Yacine Ouzzahra, Michele Filippo Fontefrancesco, Maria Giovanna Onorati, Gino Gabriel Bonetti, Tiziana de-Magistris, Torsten Bohn
Opublikowane w:
BMJ Open, Numer 14, 2024, ISSN 2044-6055
Wydawca:
BMJ
DOI:
10.1136/bmjopen-2023-083558
Autorzy:
Sarah Forberger, Lucia A Reisch, Pieter van Gorp, Christoph Stahl, Lara Christianson, Jihan Halimi, Karina Karolina De Santis, Laurent Malisoux, Tiziana de-Magistris, Torsten Bohn
Opublikowane w:
BMJ Open, Numer 14, 2024, ISSN 2044-6055
Wydawca:
BMJ
DOI:
10.1136/bmjopen-2023-080644
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