Implementing a CAPA System
Tuesday, September 23, 2014, 11:00 am Pacific / 2:00 pm Eastern
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Corrective and Preventive Action (CAPA) is one of the most challenging quality system elements that companies face during inspections and audits. CAPA is a fundamental management tool that should be used as such in every quality system by implementing better metrologies and applying effective risk-based filters. A robust and effective CAPA program is especially important for medical device manufacturers. An effective CAPA system that identifies and eliminates (potential) non-conformities enables both regulatory compliance and at the end cost savings. Join TÜV SÜD America for their webinar CAPA E-ssentials to learn more about the importance, requirements, and essential elements of a CAPA program. The webinar will also discuss common pitfalls and guidance on how to implement a CAPA system. Click here to register.