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The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.
Event date: 18/07/2024 Export event
eCF Birds-of-a-Feather Webinar: Protocol Optimization using AI/ML
Date: Thursday, July 18, 2024 Duration: One hour
Presenters: Sidd Bhattacharya, Partner, PwC
About this topic: We will be discussing the transformative potential of Artificial Intelligence (AI) and Generative AI in clinical development. This session will delve into the pivotal role of AI across the clinical trial lifecycle, focusing on use cases from protocol design, study start-up, execution, through analysis and reporting. We will explore how these technologies are not only optimizing trial efficiency, but also significantly reducing cycle-times while improving quality.
Time: We apologize for the inconvenient time for our members in the Asia Pacific time zones. We will be recording the session, so if you are unable to attend, please register to receive the recording.
Open To: All employees of eClinical Forum member companies (gratis). Please feel free to forward this invitation within your organization.
For information on eCF membership, please see www.eclinicalforum.org/membership or send an inquiry to info@eclinicalforum.org.
Background: eClinical Forum webinar sessions focus on the details of a specific topic. All participants are encouraged to share information and ask questions. Anyone from an eCF member company can participate, gratis. The eClinical Forum does not endorse any particular technology, system or platform.
What You Need to Do: Register by using this link: eCF Birds-of-a-Feather Webinar: Protocol Optimization using AI/ML (eclinicalforum.org)
What Happens Next: You should receive a confirmation of your registration immediately after registration. If you do not – then your registration did not go through and please contact webinars@eclinicalforum.org. We will send out connection instructions several days before the event to those who have registered.
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Requirements for Electronic Data for Regulated Clinical Trials - "eCF Requirements" past public releases 2018 - 2023
The eCF REG team puts out a yearly version of the "eCF Requirements" which many orgainizations use to check compliance of their systems against regulatory authority document statements. The previous versions have been requested in order to easily check the requirements that were in place in a particular year.
eCF APAC Autumn Workshop 2024 Announced
Registration is open! Our APAC Autumn workshop will be kindly hosted by Clario at the Hyatt Regency Tokyo Bayin Urayasu, Japan on November 11-12 2024.
eCF Birds-of-a-Feather Round-Table: Risk-Based Source Data Verification
This topic is coming out of a discussion that started at the eCF Workshop in Massachusetts in October. The group decided they wanted more time to delve more deeply into this discussion and to include eCF members from other regions. The discussion will be around:
eCF “Think GCP” Webinar: ICH E6(R3) for eCF Members
Presenter: Rebecca Stanbrook, GCP Strategic Lead, Process & Risk Surveillance, Novartis, EFPIA Topic Lead ICH E6(R3)
About this topic: The final piece of the GCP renovation puzzle, revision 3 of ICH GCP. Understand the background to the renovation, key changes and the philosophy of the changes in this one hour webinar.