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Thursday 30 October 2014

[New announcement] How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance

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?
http://bit.ly/1q39eXd

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

Download FREE here: http://bit.ly/1q39eXd
 
 
 
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Announcement in Pharmaceutical Jobs Biotech Life Science Healthcare Pharma & Medical Devices Careers HR Recruitment
 
 
 
 
How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance
 
announcerFullName
 
Paul Healy
Director, International Healthcare Recruitment [IHR]
 
 
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?
http://bit.ly/1q39eXd

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

Download FREE here: http://bit.ly/1q39eXd
 
 
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