﻿<?xml version="1.0" encoding="utf-8"?><!--RSS Genrated: Tue, 07 Apr 2026 07:26:21 GMT--><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:ev="http://purl.org/rss/1.0/modules/event/"><channel><title>eClinical Forum - Advisory Group</title><link>https://eclinicalforum.org:443/teams-projects/rss/category/460/advisory-group</link><atom:link href="https://eclinicalforum.org:443/teams-projects/rss/category/460/advisory-group" rel="self" type="application/rss+xml" /><description>RSS document</description><item><dc:creator><![CDATA[Suzanne Bishop (eCF Facilitator)]]></dc:creator><title><![CDATA["When should audit trail begin?"]]></title><link>https://eclinicalforum.org/teams-projects/when-should-audit-trail-begin</link><description><![CDATA[ Several members of the eClinical Forum's Regulatory Advisory Group have published an article in Applied Clinical Trials on "When should audit trail begin?"  It is a discussion of the regulatory ...]]></description><pubDate>Thu, 17 Jun 2021 14:50:00 GMT</pubDate><guid>https://eclinicalforum.org/teams-projects/when-should-audit-trail-begin</guid><dc:identifier><![CDATA[ab8edbe3-2944-49a2-aab5-6e6fd231b1cb-183]]></dc:identifier></item><item><dc:creator><![CDATA[Webmaster1]]></dc:creator><title><![CDATA[Regulatory Advisory Group (REG)]]></title><link>https://eclinicalforum.org/teams-projects/regulatory-advisory-group-reg</link><description><![CDATA[ The REG team reviews, evaluates and interprets documents from regulatory authorities. The team is comprised of regulatory professionals from all aspects of eClinical Forum (pharma, technology ...]]></description><pubDate>Tue, 01 May 2018 14:01:00 GMT</pubDate><guid>https://eclinicalforum.org/teams-projects/regulatory-advisory-group-reg</guid><dc:identifier><![CDATA[ab8edbe3-2944-49a2-aab5-6e6fd231b1cb-49]]></dc:identifier></item><item><dc:creator><![CDATA[Webmaster1]]></dc:creator><title><![CDATA[eSRA Maintenance]]></title><link>https://eclinicalforum.org/teams-projects/esra-maintenance-1</link><description><![CDATA[  eSRA Maintenance Working Group  

 eSRA (eSource-Readiness Assessment) is a questionnaire used by sites to self-evaluate their electronic systems that may originate or manage data for clinical ...]]></description><pubDate>Thu, 01 Mar 2018 11:18:00 GMT</pubDate><guid>https://eclinicalforum.org/teams-projects/esra-maintenance-1</guid><dc:identifier><![CDATA[ab8edbe3-2944-49a2-aab5-6e6fd231b1cb-50]]></dc:identifier></item><item><dc:creator><![CDATA[Webmaster1]]></dc:creator><title><![CDATA[MEMBERS: Submission of comments to FDA on Draft eSource Guidance]]></title><link>https://eclinicalforum.org/teams-projects/members-submission-of-comments-to-fda-on-draft-esource-guidance</link><description><![CDATA[ The eClinical Forum held an open discussion with members from pharma, CROs, and associated software vendors, to talk about this draft FDA guidance on Jan 8, 2013.  The resulting comments are a ...]]></description><pubDate>Tue, 12 Mar 2013 13:55:00 GMT</pubDate><guid>https://eclinicalforum.org/teams-projects/members-submission-of-comments-to-fda-on-draft-esource-guidance</guid><dc:identifier><![CDATA[ab8edbe3-2944-49a2-aab5-6e6fd231b1cb-31]]></dc:identifier></item></channel></rss>