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

  • 15 Jun 2017
  • Webinar

Description

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations 2017 is a webinar that covers topics such as:

  • 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

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations 2017 is intended for:

  • 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

Health & Medicine: Healthcare, Hospitals & Clinics, Medical technology
Industry: Food & Beverages

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