"This is the best use of my time to remain current with what is going on in the industry."
WHO WE ARE
The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.
Login to also view news for Members.
This meeting is being replaced with a Virtual Global Workshop on 11-13 May 2020.
Networking with peers has never been more important in order to stay current, collaborate on shared challenges and influence the future. The eClinical Forum offers a unique, non-commercial networking environment to learn, exchange information and ideas, collaborate on shared initiatives.
For more information on our Virtual Global Workshop, please contact email@example.com.
This webinar will share
Facilitator:Hugo Cervantes, Vice President Vault CDMS, Veeva
Learn how top pharmaceutical companies and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times.
The eClinical Forum Asia-Pacific took place in Tokyo, 5-6 November 2018, kindly hosted by Boehringer Ingelheim - Japan with many pharmaceuticals, CROs, and software vendors attending. For more information, please contact firstname.lastname@example.org
That's what one person wrote on the evaluation ... while another wrote "ECF are the only meetings I attend each year. It gives me everything I need to stay current and to answer my questions" and another wrote "People were amazing. Topics were great. Hosting and events as well." Yes, indeed it was a terrific meeting and we are already planning for follow-up discussions in our project teams, webinars and Spring meetings. Thank you to all who participated!! And a special Thanks for Servier for hosting us. The meeting was attended by: Merck KGaA, ZeinCRO, eResearch Technology, Munich Technical University, Hoffman La-Roche, TriNetX, BSI Business Systems Integration, Orion, Novartis, DBV Technologies, Medidata Solutions, Oracle, CRF Health/Bracket, DMB, Boehringer-Ingelheim, Janssen Pharmaceuticals, Idorsia, Actelion, Ferring, Assistance Publique-Hopitaux de Paris, Wega Informatik, Novo Nordisk, Royal Cornwall Hospitals NHS Trust, 23 Consulting, Neptunus Data, and of course Servier.
NOT A MEMBER?
We wish you a Happy New Year 2021
Background vector created by YusufSangdes - www.freepik.com
Birds-of-a-Feather Round Table Discussion: New recommendations from EMA on the frequency of investigators’ signature collection on eCRF data
In July 2020, EMA released a new Q&A to provide further expectations on continuous oversight and frequency of investigators’ signature collection on eCRF data reported to the sponsor. Prior to filing a marketing authorization application, all eCRF data should be signed and dated. But also important data such as that related to reporting of SAEs, adjudication of important events and endpoint data, DSMB review, should be signed off in a timely manner. In addition, a timely review and sign-off of data that are entered directly into the CRF as source is particularly important.
The intent of this webinar is to identify if there are new challenges, and if any – to proceed with an update to the eCF best practices on investigator signatures document that was released in 2017.