Checkout 0
Training Courses - Web Seminar Archives

Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.

Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).

Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.

Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.

Archive: Source Documentation: What is Adequate and Accurate?

Course #: BI13743
January 15, 2020

Course Description

Lack of adequate and/or accurate source documentation has been noted as a common deficiency in inspection findings of Clinical Investigators, andregulators report that quality source documents reinforce quality site data. Regulatory requirements (FDA, ICH) will be reviewed in this web seminar. Further, the following topics will be covered: Variability of stakeholder requirements (sponsor-to-sponsor, per study, sponsor to site), case report forms (CRFs) as source data, electronic medical records, shadow charts, source document worksheets, protocol deviations, telephone and email contacts, good documentation practices, making corrections to source documents, late entries, back-dating (oh no!), and details of FDA inspection methods and findings regarding source documents. Leading practices will be discussed to assist sites with implementing the regulatory requirements for source documents. 

Video Preview


Learning Objectives

  • Define source data and source documents
  • Identify regulatory required characteristics of source data and source documents
  • Identify three attributes of source document worksheets
  • Describe three attributes of ALCOAC (attributable, legible, contemporaneous, original, accurate, complete) for source documents
  • Discuss CRFs as source data

Who Should Attend

  • Site Research Directors/Managers
  • Clinical Research Coordinators
  • Principal Investigators
  • Clinical Research Associates
  • Project Managers
  • Clinical Research Associate Managers
  • Quality Assurance Personnel


Marla Hoelle, R.N., B.S.N., C.C.R.A.-PM., P.M.P.

Click here for complete trainer biographies


Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.