Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan 2012

  • 07 Dec 2012
  • Webinar

Description

Topics
  • Elements of Monitoring
  • Elements of Quality Assurance Program
  • Roles and responsibilities of study team members
  • Elements of Auditing
  • Implementing change
  • Training and Education requirements
Who should Attend
  • Experienced Principal Investigators
  • Experienced Clinical Research Coordinators
  • Site Based Clinical Research Managers and Administrators
  • Experienced Clinical Research Associates (Monitors)
  • Regulatory Compliance Associates and Managers

Past Events

Important

Please, check "Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical laboratories, Pharma
Science: Life Sciences & Biology

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