Webinar: Clinical trial results reporting on EudraCT made easy
Focus: Posting results for trials completed before 21 July 2013 or trials that were ended prematurely
Thursday, 17th of February 2022, 15:00-16:30 CET (Berlin time)
Recordings of the Event
The recording from the Webinar Clinical trial results reporting on EudraCT made easy (Focus: Posting results for trials completed before 21 July 2013 or trials that were ended prematurely) (February 17th, 2022) can be found here.
This webinar will give practical skills for reporting clinical trial results on the European registry EudraCT, focusing on trials that were completed before 21 July 2013 and trials that were prematurely ended. It is possible to upload results for these trials using a simplified process. For institutions that want to improve their EudraCT reporting, uploading results for these trials is a good first step.
Target group
Target group:
People who manage data and/or upload trial results onto EudraCT, including clinical trial unit staff, research governance staff, and trial and project managers.
Previous knowledge:
Beginners and experienced persons
| Time | Speaker | Topic | |
|---|---|---|---|
| 15:00-15.15 |
Dr. Britta Lang, KKS-Netzwerk e. V. Dr. Anette Blümle, Zentrum Klinische Studien, Universitätsklinikum Freiburg, Germany |
Introduction: webinar goals, background Simplified processes for: 1. Trials completed before July 2013 2. Prematurely ended trials How to manage copyright issues | |
| PART ONE: REPORTING OF EXPERIENCES | |||
| 15:15-16:00 | Dr. Kerstin Bollweg, Clinical Trial Office, Charité - Universitätsmedizin Berlin, Germany |
Demonstration of how to upload results, and tips and tricks. - How to identify all relevant trials at my institution? - How do I successfully contact researchers? - What steps can I take on behalf of the researchers? - How specifically do I upload papers from the affected studies? - How do I deal with inconsistent data? | |
| PART TWO: QUESTIONS & FURTHER EXCHANGE | |||
| 16:00-16:25 | All | Q&A and discussion | |
| 16:25-16:30 |
Dr. Britta Lang, KKS-Netzwerk e. V. Dr. Anette Blümle, Zentrum Klinische Studien, Universitätsklinikum Freiburg, Germany | Wrap-up and plans for future webinars |
[Translate to englisch:] Programme
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Webinar Programme
Download, Pdf (47 KB)
The webinar will be held online and in English language. Registered participants will receive the log in details beforehand.
Materials to prepare for the webinar:
- QUEST clinical trial reporting manual
- Background on how to manage copyright issues: Oxford Academic Author self-archiving policy and Lippincott Journal Portfolio Author Permission Guidelines
Number of participants:
To enable discussions and exchanges of experience, the number of participants will be limited to 25.
Costs:
The course is free to attend.
Organizers and hosts
Host: BIH QUEST Center for Responsible Research, together with the European University Hospital Alliance (EUHA), the KKS-Netzwerk e.V..
Organizer: Consilium Scientific
Important information
Date: Thursday, 17th of February 2022, 15:00-16:30 CET (Berlin time)
Course language: English
Registration:
Registration is closed.
The number of participants will be limited to 25. We will allow more registrations in order to obtain as even a distribution as possible among different countries. Registered persons will receive a confirmation of their participation incl. login data by Consilium Scientific in due time.
