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

Principal Investigators’ Signatures 04 March 20210

Principal Investigators’ Signatures

Aligning the existing eCF best practices document with the most recent regulatory expectations

eConsent 17 October 20190


Evaluating the currently available data on the implementation of Electronic Consent

Audit Trail Review 29 January 20190

Audit Trail Review

Best practices for meeting regulatory expectations for Audit Trail Review

PI Signatures - ENDED 02 November 20160

PI Signatures - ENDED

Evaluating regulations and guidances pertaining to principal investigator signatures on study data and materials

EDC Hosting - ENDED 26 November 20130

EDC Hosting - ENDED

Best practices for data transcribed to electronic data collection tools

Risk-Based monitoring - ENDED 15 May 20120

Risk-Based monitoring - ENDED

Best practices for ensuring clinical data quality

EHR4CR - ENDED 15 March 20110


Re-use of Electronic Health Records for Clinical Research