Structure research dossier in CTIS
The application dossier consist of a Part I and a Part II. The list of required documentation and information is set out in Annex I of the CTR.
The documents in the clinical trial application should be in a searchable format.
Furthermore, it is strongly recommended to adhere to the structure of CTR Annex I when titling your documents in CTIS. Please use the codes and filenames as given in the Document codes and titles in CTIS of the Clinical Trial Coordinating Group (CTCG).
The document below contains instructions on uploading new or modified documents in CTIS, responding to an RFI, and resubmitting an application.
The following checklist contains instructions and advice on specific documents in the application. Carefully read these instructions before submitting your application, so that there is still sufficient time for adjustments.
Explanatory notes and templates (including national requirements) are given in the sections Form and MSC, Research dossier part I and Research dossier part II.
See EMA CTIS training module 10 on how to create, submit and withdraw a clinical trial.