18Mar2021 Public Release: Electronic Informed Consent Implementation Guide Practical Considerations Version 1.0 18 March 2021 Read more Public Release: Electronic Informed Consent Implementation Guide Practical Considerations Version 1.0 The EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased to announce the publication of the eConsent Implementation Guide (version 1). The joint task force was formed in 2019 with a view to look at some of the... Documents to download Electronic Informed Consent Implementation Guide Practical Considerations Version 1.0 _ March 2021(.pdf, 1.71 MB) - 2942 download(s) Read more
1Oct2019 Prominent Industry Magazines address the need for investigator site systems assessment and eSRA 01 October 2019 Read more Prominent Industry Magazines address the need for investigator site systems assessment and eSRA Documents to download Determining if Data from Electronic Health Record Systems Can Be Trusted in a Clinical Trial Setting(.pdf, 967.43 KB) - 1650 download(s) Read more
22Dec2016 White Paper, Checklist and Task Ownership Matrix for Electronic Data Capture Systems in Clinical Trials using Service Providers 22 December 2016 Read more White Paper, Checklist and Task Ownership Matrix for Electronic Data Capture Systems in Clinical Trials using Service Providers The eCF EDC Hosting Team has released the final White Paper documenting best practices for establishing controls and operational procedures that facilitate compliance with evolving regulatory expectations for Electronic Data Capture in Clinical Trials... Documents to download 01_Position_Paper_eCF_EDC_Hosting_TF_FINAL_Publish(.pdf, 1.19 MB) - 1745 download(s) 02_EDC_Hosting_Checklist_eCF_Hosting_TF_FINAL_Publish(.pdf, 733.27 KB) - 1387 download(s) 03_Task_Ownership_Matrix_eCF_Hosting_TF_FINAL_Publish(.pdf, 736.89 KB) - 1616 download(s) Read more
2Mar2016 Is your electronic health record system suitable for originating records that will be used in regulated clinical trials? 02 March 2016 Read more 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... Documents to download ACRP_ProfDev_Webinar_eCF_eSRA_Feb_10_2016_Final(.pdf, 1.62 MB) - 2088 download(s) Read more
3Dec2015 2001 to 2009: Investigational Site Perspectives on Clinical Trial Information Systems - Sep 2012 03 December 2015 Read more 2001 to 2009: Investigational Site Perspectives on Clinical Trial Information Systems - Sep 2012 Abstract In 2001, a survey was conducted by the eClinical Forum to explore the experience, needs, views and issues of investigational site staff with respect to Electronic Data Capture (EDC). Documents to download eCF_Site_Survey_2009_ARTICLE_18_September_2012(.pdf, 1.52 MB) - 1109 download(s) Read more
10Sep2013 Risk-Based Approaches - Best practices for ensuring clinical data quality 10 September 2013 Read more Risk-Based Approaches - Best practices for ensuring clinical data quality Companies engaged in commercial clinical research have, since the introduction of formalized good clinical practices (GCP), adopted highly defensive practices around the monitoring of clinical trials. Documents to download Risk_Based_Approach_Best_Practices_Final_Peer_Review_(Version_Upload_2)(.pdf, 424.31 KB) - 763 download(s) Read more