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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.

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eClinical Forum Europe Meeting in Paris, France 23-25 October 2018

"Excellent, open discussions on current priority topics"

  • 10 September 2018
  • Author: Webmaster1
  • Number of views: 2852

Event date: 10/23/2018 - 10/25/2018 Export event

eClinical Forum Europe Meeting in Paris, France 23-25 October 2018

2018 Autumn European meeting will be held at Servier in Paris, France on 23-25 October 2018.

Meeting Venue: Servier, 50 rue Carnot, 92284 Suresnes Cedex, France

Who Should Attend

This meeting will be of relevance to those with an interest in advancing clinical research from:

  • Clinical Trial sponsor organisations
  • Healthcare institutions
  • Technology providers
  • Service providers
  • Academia
  • Stakeholder groups and associations
  • Government

About the Meeting

Networking with peers has never been more important in order to stay current, collaborate on shared challenges and influence the future.

The eClinical Forum offers a unique, non-commercial networking environment to learn, exchange information and ideas, collaborate on shared initiatives.

The following topics will be covered during the meeting:

  • Clinical Trial Operations:
    • Feasibility
    • Patient recruitment
    • eInformed Consent
    • SAE collection and reconcilliation
    • Clinical Trial transparency
  • Regulatory Trends:
    • FDA: Use of Electronic Health Record Data in Clinical Investigations
    • PI Signatures – considerations for EDC and non-EDC data
    • Archiving and Decommissioning
    • Streamlining validation
  • Emerging Technologies/Processes:
    • Blockchain: A clinical research implementation
    • Artificial Intelligence/Machine learning: Case study
    • FHIR Standards
    • Business Intelligence Reporting Tools -- how companies are making sense of complex data
    • Secondary use of anonymized patient data
    • Following the patient journey
  • Workshop: Defining the attributes of the Trial of the Future
  • Workshop: It is reported that only 50% of investigators do more than one trial. Understanding the statistic.
  • eCF Project Teams: Progressing shared initiatives

Documents to download

Categories: EVENTS, Europe Meetings
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«April 2020»
4/21/2020 UTC

Birds-of-a-Feather Round-Table Webinar Discussion: Subject Status Calculations

Facilitator: Lisa Jones-Moore, Clinical Systems & Supplies Planning, Eli Lilly & Co.

This is a round-table discussion and participants are encouraged to share their experiences, ideas and questions on this topic.

The following questions will be discussed:

  • How many subject/patient dispositions do you collect (i.e. Subject completed treatment and follow-up, Subject discontinued treatment and dropped follow-up, Subject discontinued treatment and completed follow-up, etc.)
  • How does subject status get updated in your clinical trial management system?  Automated calculation using a datahub or manual update by monitoring or other personnel?
  • Is monitoring done internally or is there a third party organization performing this task?  If TPO, do they use their own system or your system?  If they use their own system, how does the data get back into your system?
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