Draft stewardship plan
(si apre in una nuova finestra)
The stewardship plan outlines how to achieve the optimal use of an intervention, including, for example, how to avoid irrational use, overuse or abuse of health technologies
Study initiation package
(si apre in una nuova finestra)
The study initiation package will include the following information from the beginning of the trial:• 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 required for the enrolment of the first study participant (In case of multicentre clinical studies, submission of approvals for the first clinical site is sufficient)Th study intiation package will also include: • The submission of the updated protocol with new progress plan and dates • The ethics extension and approval letters from relevant national bodies
Midterm Recruitment Report
(si apre in una nuova finestra)
This report is due 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 delays.
Exploitation and dissemination plan
(si apre in una nuova finestra)
English Word file on a revised and updated exploitation and dissemination plan will be submitted.
Collection of documents related to the status of the clinical trial
(si apre in una nuova finestra)
PDF consisting of the collection of documents related to the status of the clinical trial
Updated Project Plan
(si apre in una nuova finestra)
A final English Word document outlining the updated project’s implementation phase and timeline.