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Recorded Webinar
CAPA and Critical Documentation of Clinical Trial Activities During and Post COVID-19 Restrictions
timelapse 60 Min with 15 Min QnA of Q and A
Note:
This webinar occured in the past
Along with recorded webinar, copy of presentation slides will be shared
Recorded Webinar can be played unlimited times
Speaker/Presenter
Biopractice
Short Abstract
This course discusses the need for quality documentation of events that occurred during the crisis that are linked to significant risks and issues that matter. You will review important actions and documentation between various stakeholders (read: sites and sponsors, CROs and sponsors, etc.) which must happen to ensure deviation identification, root cause analysis (RCA), and Corrective and Preventative Actions (CAPA) are handled in a compliant fashion. Best practices for remote implementation of these activities will be discussed. This course will also provide guidance to conduct “renovations” to your existing quality systems to ensure oversight and adequate monitoring and quality conduct of your trial.
The presentation will cover the following areas:
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