U.S. FDA Corrective and Preventative Action (CAPA) for Medical Devices

Dec 7th, 2006
London, --
GB
https://www.management-forum.co.uk
More than 50% of FDA's 483 Observations and Warning Letters are Corrective and Preventative Action (CAPA)-related. This one-day seminar will address the requirements and expectations of CAPA to meet the U.S. FDA medical device requirements.
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