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Links zu Ergebnissen und Veröffentlichungen von RP7-Projekten sowie Links zu einigen Typen spezifischer Ergebnisse wie Datensätzen und Software werden dynamisch von OpenAIRE abgerufen.
Leistungen
Project website is updated and newsletters are sent out
Project website (öffnet in neuem Fenster)Project website is launched at the start of the project
Refresher trainings are organised to ensure project and health staff is able to operateaccording to the project’s guidelines and clinical standards
Data analysis plan (öffnet in neuem Fenster)A data analysis plan for the overall study data is developed
Communication plan (öffnet in neuem Fenster)Communication plan is updated and shared with project partners
National progress meetings 1 (öffnet in neuem Fenster)National progress meetings with relevant project stakeholders are organised on country-level
Refresher trainings 1 (öffnet in neuem Fenster)Refresher trainings are organised to ensure project and health staff is able to operateaccording to the project’s guidelines and clinical standards
International Steering Committee Meetings 1 (öffnet in neuem Fenster)Ensure that the project’s scientific steering committee meetings are organised and feedback and input is gained
Midterm recruitment report (öffnet in neuem Fenster)When 50% of the study population is recruited. The report shall include an overview of the number of recruited participants by clinical sites, any problems in recruitment and, if applicable, a detailed description of implemented and planned measures to compensate for any incurred delay.
Scientific code of conduct (öffnet in neuem Fenster)A scientific code of conduct for the project is developed/updated and endorsed by all consortium partners
Plan for dissemination and exploitation of results (öffnet in neuem Fenster)Plan is developed and shared with project partners
Updated plan for dissemination and exploitation of results (öffnet in neuem Fenster)Plan is updated and reshared with project partners
Report on the status of posting results 1 (öffnet in neuem Fenster)Summary results posted in the applicable registry/ies (where the study was registered)
Reports of monitoring trips 1 (öffnet in neuem Fenster)Once per year the country-level coordinating team will visit the health centres included in the project
Consortium meetings 1 (öffnet in neuem Fenster)Annual consortium meetings are organised to align all project partners
Data Management Plan (öffnet in neuem Fenster)A data management plan for the overall study is developed
Updated Data Management Plan (öffnet in neuem Fenster)The data management plan is updated
Impact of COVID-19 at a national level (öffnet in neuem Fenster)Report on the impact of COVID-19 on the PEP4LEP study per implementing country
Registration number of the clinical study in a registry meeting WHO Registry criteria; Final version of study protocol as approved by the regulator(s) / ethics committee(s); Regulatory and ethics (if applicable, institutional) approvals (or amendments if applicable) required for the enrolment of the first study participant (with multicentre clinical studies, submission of approvals for the first clinical site is sufficient)
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