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eCF BoF Round-table: Utilization of Scribes for eCOA

15-June-2021

Event date: 15/06/2021 Export event

eCF BoF Round-table: Utilization of Scribes for eCOA

Birds-of-a-Feather Round Table Discussion:  Utilization of Scribes for eCOA

Date:  Tues 15-June-2021       Duration: One hour

Presenter:   Christy Schechter, Eli Lilly

Open To: Staff from eClinical Forum member companies gratis  (If you are not an eCF member, please review our website www.eclinicalforum.org/membership for membership information or contact 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 facilitator will [try to] keep the subject on track and prompt discussion and information sharing.

For This Topic:  This is a round-table discussion. Participants are encouraged to share experiences, make comments, ask questions, and contribute to the discussion. We will be discussing “The utilization of scribes is needed for the conduct of clinical assessments within eCOA.  Therefore, eCOA needs to be built in a manner that meets the regulatory requirements for scribing, to ensure all individuals participating in the assessment are audit trailed.”

Time – this webinar is offered at 2 times, both on 15-June-2021. We hope you will find one of them convenient for your participation.  Webinar A: UTC 07:00, Webinar B: UTC 15:00

MEMBERS -- FOLLOW THIS LINK TO REGISTER:  Webinar Registration (eclinicalforum.org)

NON-MEMBERS -- Please see information on membership in the Membership tab on this website or contact info@eclinicalforum.org for more information.

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eCF Free Public Webinar: Regulatory Requirements for Electronic Data/Systems for Clinical Trials, and associated site system assessments

eCF Free Public Webinar: Regulatory Requirements for Electronic Data/Systems for Clinical Trials, and associated site system assessments

The eClinical Forum is pleased to offer a free public webinar – to provide information on our 3 free tools: The “eCF Requirements” (Requirements for electronic data for regulated clinical trials), eSRA (Site eSource-Readiness Assessment), and ISF (Investigator Site File System) Assessment. 18-Sept-24: Registration Required.

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