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Technology Showcase: "Can a full-featured EDC be out-of-the-box?"

29-March-2017; Registration Required

Event date: 3/28/2017 Export event

Technology Showcase: "Can a full-featured EDC be out-of-the-box?"

Technology Showcase: Can a full-featured EDC be out-of-the-box?

Date and Time: Wed, 29 March 2017         Duration: One hour

Time: UTC 1400; 15:00 CET, 09:00 AM EST, 9:00 PM Singapore. We apologize for the inconvenient time in some regions.


Presented by: Target Health Inc.-- Jules Mitchel, Joonhyuk Choi, Yong Joong Kim and Les Jordan

Open To: Staff from eClinical Forum member companies


Background: This is an eClinical Forum Technology Showcase. Our Technology Showcase sessions have been requested by eCF members to provide a demonstration of products or services, and by necessity are not technology or vendor neutral. The eClinical Forum does not promote nor endorse any particular technology vendors. Any member can participate that has an interest in the topic area. The facilitator will [try to] keep the subject on track and prompt discussion and information sharing.

For This Topic: Now that paper records are disappearing from the clinical trial landscape, functionalities of the clinical trial enterprise should be easily available at one website and with one login.  While documents can sit in the trial master file (TMF), access to the EDC system should be seamless from the time that the patient electronically signs the informed consent form (eICF).  Drug supply management, randomization, SAE reporting, coding, central and onsite monitoring reports, RBM, data management, database lock, etc., and even integration with the electronic medical record can be managed all at one website. (Plug-ins with specialized software features like EEG and CGM integration may need some one-off custom programming.)  Join us as we discuss the voyage of the paperless clinical trial.  

What You Need to Do: Register using the link:  https://www.surveymonkey.com/r/Out-of-the-box-EDC

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eCF Birds-of-a-Feather Webinar: Use of eCOA Metadata to Detect Fraud, Develop Risk Indices and More

Electronic solutions for patient-reported and clinician-reported outcomes provide rich metadata that can be mined for additional insights describing trial performance and driving risk-based monitoring. We will explore the use of this eCOA meta data in fraud detection, and other analytics insights and how these data might translate to risk indices to inform risk-based monitoring activities.

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