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How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance
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"How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance"
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If your company is a sponsor or a CRO that conducts clinical research for a sponsor, how effective are your risk management and clinical CAPA processes? Are you using a risk-based approach to monitoring and CAPA to mitigate the risks during clinical research and ensure compliance?

This white paper will discuss the importance of risk-based monitoring and CAPA in clinical research within the context of the following initiatives by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA):

  • 2013 Guidance
  • Clinical Trial Transformation Initiative (CTTI)
  • EMA's Reflection Paper on Risk-Based Quality Management in Clinical Trials


Offered Free by: MasterControl Inc.
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