Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations 2017

  • 08 May 2017
  • Webinar

Description

Topics
  • Using EHRs that are interoperable with electronic systems supporting clinical investigations
  • Whether and how to use EHRs as a source of data in clinical investigations
  • Ensuring that the use of EHR data collected and used as electronic source data in clinical investigations meets FDA`s inspection, record keeping and record
  • Ensuring the quality and integrity of EHR data that are collected and used as electronic source data in clinical investigations
  • Retention requirements
Who should Attend
  • Clinical Investigators (physicians)
  • Ponsors of clinical trials (drug, biologic, medical device & combination product manufacturers)
  • Institutional Review Boards (IRB) / Ethics Review Boards (ERB) / Research Ethics Boards (REB)
  • Contract Research Organizations (CROs)

Past Events

Important

Please, check "Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations" official website for possible changes, before making any traveling arrangements

Event Categories

Education: E-learning, Education Technologies & Methods, Training
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical technology

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