A vast majority of the current industry deficiencies which have led to isolated 483s, Warning Letters and Consent Decrees are the result of deficient technical documentation and effective means of assessing various elements of CAPA expectations for products produced and distributed under the FDA regulations.
CAPA Training and Causes of Warning Letters due to Lack of Comprehension - Webinar By GlobalCompliancePanel
23 April 2013, Fremont, United States
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Livermore Common, Online Training, California, Fremont, 94539, United States
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