WebJan 31, 2024 · EudraCT step-by-step guide For a trial conducted in the European Economic Area: As of 31 January 2024, all initial trial applications in the European Union (EU)/European Economic Area (EEA) must be submitted through CTIS. WebJan 31, 2024 · Register for a user account in EMA Account Management portal In order to gain access to the CTIS sponsor workspace, all users will require to have an active EMA account. Users who already have access to other EMA applications e.g., Eudralink, Eudravigilance can access the CTIS system using their existing EMA account credentials.
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WebFeb 7, 2024 · Participants receive access to the CTIS training environment and will practice basic functionalities during the live training course. Feb 07, 2024 9:00 AM – Feb 10, 2024 1:30 PM (Central Europe Standard Time) Virtual List price: €1665 Register Now (Credit Card) This course is now fully booked! WebOct 19, 2024 · October 19, 2024. Author (s): Lidya Dominguez, BS. CTIS go-live is just around the corner. The new portal brings a new approach to clinical trials in the … reach font
Mandatory Use of Clinical Trial Information System (CTIS) for …
WebCTiS2024 Conference Registration 8th and 9th July 2024 at IISER, Pune. CSpathshala proudly announces the fourth conference on Computational Thinking in Schools … WebJan 11, 2024 · Primary Registries in the WHO Registry Network meet specific criteria for content, quality and validity, accessibility, unique identification, technical capacity and administration. Primary Registries meet the requirements of the ICMJE. The registries that currently meet these criteria are: WebJan 31, 2024 · Search in the EU Clinical Trials Register Information on clinical trials A clinical trial is a study performed to investigate the safety or efficacy of a medicine. For human medicines, these studies are carried out in human participants (either patients or healthy volunteers). how to sprint in anime rifts