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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.

 

NEWS FROM THE ECF

eCF "Birds-of-a-Feather" Round-table Discussions and Technology Showcases 2020 to 2021

Select recordings available

eCF "Birds-of-a-Feather" Round-table Discussions and Technology Showcases 2020 to 2021

“Birds-of-a-Feather” Webinars are provided monthly, to get those with similar interests together.  Anyone from an eCF member company (around the globe!) can participate, gratis. All eCF members can suggest a topic and/or lead a discussion.

The following topics were discussed in 2020 and 2021. Those with an asterisk * have been recorded, and are available to eCF members, upon request. Please send a note to webmaster3@eclinicalforum.org if you would like to view one of these recordings.

  • Tufts/eCS Survey: Data Strategy Transformation *
  • Agile Development for Clinical Research Software *
  • Real World Evidence and Real World Data *
  • Technology Showcase: Automating the Clin Data Pipeline / eClinical Solutions *
  • US National Patient Identifier
  • eSRA Japanese Language Webinar (Public) *
  • Audit Trail Review
  • Master Protocols
  • IMI Mobilise-D *
  • Technology Showcase: Lessons learned from a Covid19 Paperless Trial / Target Health *
  • Investigator Signature / regulatory authority expectations
  • eCF Brews & News “#NoGoingBack”
  • Data Archival at Sites Using Direct Download
  • eConsent – Practical Considerations in Implementing *
  • “When does Audit Trail begin?”
  • Public Webinar: “eCF Requirements” and “eSRA” *
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2021
BoF Round-Table Discussion: "eClinical Standards - Best practices for implementing"

BoF Round-Table Discussion: "eClinical Standards - Best practices for implementing"

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: “Can we develop best practices for implementing standards across sponsors and CROs of all sizes to drive efficiencies that result in medical advancements getting to patients faster?”

  • Can we facilitate a mechanism to share standards across organizations to avoid process changes from one trial to the next?
  • Can we track standard utilization across organizations to be data driven about when and how updates are needed?
  • With the increase in digital trials, what additional standards should we be considering?
  • What does an optimal standards committee look like? 
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