Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013

  • 06 Feb 2013
  • Webinar

Description

Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013 is a webinar that covers topics such as:

  • Way to ensure human subject protections
  • The importance of investigator-initiated trials
  • What are the site responsibilities in investigator initiated trials
  • The investigator deficiencies
  • The resources available to help the investigator in the conduct of investigator-initiated trials
  • The approaches or concerns of Institutional Review boards

Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013 brings together:

  • Senior Clinical Research Associates(CRAs)
  • Principle Investigators
  • Contract Research Organizations (CROs)
  • Clinical Research Project Manager
  • Site Management Organizations (SMOs)
  • Institutional Review Boards (IRBs)

Past Events

Important

Please, check "Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection?" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical laboratories, Pharma

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