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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.


News from the eCF

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Webinar: Incorporating Visual Learning into Clinical Research

eCF Technology Showcase: 23-Jan-2017 - Registration Required

Event date: 1/22/2017 Export event

Webinar: Incorporating Visual Learning into Clinical Research

Incorporating visual learning into clinical trials

Jan 23, 2017: 

Time: One hour, starting at 9am New York, 1500 Paris, 10pm Singapore  (UTC/GMT: 1400)

We will discuss the following:

• Benefits to presenting information visually and why it can be a more effective way to share complicated data sets

• The growing complexity in clinical trials and how aggregating multiple data streams into a visual format may help drive earlier recognition of patterns and events

• Examples of how clinical teams and have used visualizations to create understanding and drive communication across functions

• Visual reports that can support new industry approaches such as Risk Based monitoring

 

This webinar is free for eCF members. Registration via this link: https://www.surveymonkey.com/r/eCF_Visual_Learning

Non-eCF Members can request additional information via a note to info@eclinicalforum.org

 

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 or technology vendor. 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. 

 

 

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2/11/2020 UTC

eSRA: Can Your Site Electronic Health Record Systems (EHR) be Used to Source Clinical Research Data?

This presentation on the eClinical Forum's eSRA (eSource Readiness Assessment) will be given by Martijn Griep, eClinical Forum Representative & Associate Director, Janssen, The Netherlands. It will be on Feb 11, 2020 at 15:00

More information on this conference can be found at: https://eucrof-conference.eu/programme/  

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2/25/2020 - 2/26/2020 UTC
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Free Public Webinar: Sponsor responsibility to Assess Investigator Site Systems that may originate source for clinical trials & the free eSRA tool

Presenter:  Kelley Olree, Study Manager – Pfizer, and eClinical Forum eSRA Team

This webinar will discuss:

  • What the Sponsor’s responsibility is regarding using data that has originated in an Investigator Site system (Electronic Health Records (EHR) or Electronic Medical Records (EMR) according to different health authorities
  • Benefits of all sites and all sponsors and all CROs using a common assessment tool
  • The eClinical Forum, a non-profit, non-commercial discussion/action group comprised of members of the Pharmaceutical and Clinical Research Services industry, along with sites and academia, have developed a regulatory-based assessment tool for clinical research sites to determine if their computer system (EHR, EMR, etc) is appropriate to hold regulated clinical trial data. It has been available for free for over 4 years and is currently being used around the globe by many sponsors and thousands of sites.
  • The eClinical Forum’s free “eSource-Readiness Assessment” (eSRA) that assists the sponsor/site in determining if the site system is appropriate for sourcing clinical research records
  • How a Sponsor/CRO can incorporate eSRA into their processes
Read more
26
2/25/2020 - 2/26/2020 UTC
93

Free Public Webinar: Sponsor responsibility to Assess Investigator Site Systems that may originate source for clinical trials & the free eSRA tool

Presenter:  Kelley Olree, Study Manager – Pfizer, and eClinical Forum eSRA Team

This webinar will discuss:

  • What the Sponsor’s responsibility is regarding using data that has originated in an Investigator Site system (Electronic Health Records (EHR) or Electronic Medical Records (EMR) according to different health authorities
  • Benefits of all sites and all sponsors and all CROs using a common assessment tool
  • The eClinical Forum, a non-profit, non-commercial discussion/action group comprised of members of the Pharmaceutical and Clinical Research Services industry, along with sites and academia, have developed a regulatory-based assessment tool for clinical research sites to determine if their computer system (EHR, EMR, etc) is appropriate to hold regulated clinical trial data. It has been available for free for over 4 years and is currently being used around the globe by many sponsors and thousands of sites.
  • The eClinical Forum’s free “eSource-Readiness Assessment” (eSRA) that assists the sponsor/site in determining if the site system is appropriate for sourcing clinical research records
  • How a Sponsor/CRO can incorporate eSRA into their processes
Read more
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