LEVERAGING KNOWLEDGE - DRIVING PERFORMANCE - DESIGNING THE FUTURE

Clinical Forum Teams work extensively with industry, healthcare organisations, academia regulators to link stakeholders and to facilitate the development of the environment for electronic clinical research. We have conducted surveys, developed tools, built an extensive base of knowledge of information relevant to the successful implementation of eClinical solutions.

Join the eClinical Forum to participate in cross-industry initiatives and to benefit from early access to pre-competitive information on best practices and trends.

ECF Teams and Projects

eCF Webinar on "eCF Requirements" and "eSRA" - Recording Available Here 05 May 20210

eCF Webinar on "eCF Requirements" and "eSRA" - Recording Available Here

This webinar recording provides the same content as was presented to the FDA CDER Health IT Board on 6-April-2021. Even in 2024, the content is still relevant.

Is your electronic health record system suitable for originating records that will be used in regulated clinical trials? 02 March 20160

Is your electronic health record system suitable for originating records that will be used in regulated clinical trials?

Nearly 200 attendees participated in a webinar delivered by the eClinical Forum for ACRP.

The objective of the webinar was to allow attendees to:

  • Recognize the need to assess their electronic healthcare system to determine its appropriateness for originating and/or housing data that could be used in a regulated clinical research trial
  • Access a free tool to assist in assessing electronic health record systems
Site Survey Presentation - DIA Clinical Forum Lisbon 13 Oct10 03 December 20150

Site Survey Presentation - DIA Clinical Forum Lisbon 13 Oct10

Revisiting the eClinical Paradigm

Investigational Site Perspectives on Clinical Trial Information Systems

 

As the healthcare and pharmaceutical technology spheres move closer together at the clinical research interface, the eClinical paradigm needs to be revisited in order to leverage emerging political, cultural, procedural and technological opportunities. Understanding investigational site experiences with today’s clinical trial technologies and their perspectives on future requirements is critical to delivery of improved eClinical solutions.

EHR4CR: An Innovative Platform and Business Model for Re-Use of EHR for Clinical Research (ACDM UK 10Mar14) 03 December 20150

EHR4CR: An Innovative Platform and Business Model for Re-Use of EHR for Clinical Research (ACDM UK 10Mar14)

Improved access to patient data is key to managing bottlenecks in clinical research. The presentation gives an overview of one of the largest public-private partnerships aimed at providing adaptable, reusable and scalable solutions for re-using patient level data from Electronic Health Record systems for Clinical Research.

eSRA: A Project to Self-Evaluate the GCP Compliance of Systems Holding Source Data for Clinical Trials (ACDM UK 10Mar14) 03 December 20150

eSRA: A Project to Self-Evaluate the GCP Compliance of Systems Holding Source Data for Clinical Trials (ACDM UK 10Mar14)

Investigators are frequently asked to complete sponsor-specific assessments of their EHR systems to enable sponsors to evaluate clinical trial data that will be sourced from these systems.

Investigator Site eSource-Readiness Assessment Tool 09 August 20130

Investigator Site eSource-Readiness Assessment Tool

The eClinical Forum eSource Sub-team is working on a common assessment tool to determine Investigator Site eSource-Readiness.

EHR4CR - A new technological platform enabling the re-use of data from electronic health records 12 March 20130

EHR4CR - A new technological platform enabling the re-use of data from electronic health records

CASE STUDY EHR4CR - A new technological platform enabling the re-use of data from electronic health records.

Risk Based Approaches: Best Practices for Ensuring Clinical Data Quality WEBINAR Slides Feb 2013 22 February 20130

Risk Based Approaches: Best Practices for Ensuring Clinical Data Quality WEBINAR Slides Feb 2013

Webinar slides discussing the work of the eClinical Forum "Risk Based Monitoring" Subteam. Public webinar on 22-Feb-2013. 

Leveraging EHR Data to Improve Clinical Research - Informa Brussels 25May11 08 June 20110

Leveraging EHR Data to Improve Clinical Research - Informa Brussels 25May11

Leveraging EHR Data to Improve Clinical Research - Informa Brussels 25May11

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