FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management decisions and strategy. You will learn how to use the FDA's health risk criteria so you can develop effective recall procedures. One critical aspect of recalls involves the identification of the root cause of the recall and how you could or should prevent that problem from happening again. Your corrective and preventive action program (CAPA) and quality assurance functions require a rigorous approach to prevent a chronic

Date : 3rd August 2017 to 4th August 2017

Place : United States, Salt lake city

Website :https://www.eventbrite.com/e/fda-recalls-before-you-start-and-after-you-finish-com-tickets-33510485765?aff=NDT

Contact Person:Paula Edwards

Description:

FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management decisions and strategy. You will learn how to use the FDA's health risk criteria so you can develop effective recall procedures. One critical aspect of recalls involves the identification of the root cause of the recall and how you could or should prevent that problem from happening again. Your corrective and preventive action program (CAPA) and quality assurance functions require a rigorous approach to prevent a chronic

FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management decisions and strategy. You will learn how to use the FDA's health risk criteria so you can develop effective recall procedures. One critical aspect of recalls involves the identification of the root cause of the recall and how you could or should prevent that problem from happening again. Your corrective and preventive action program (CAPA) and quality assurance functions require a rigorous approach to prevent a chronic will be held in Salt lake city,United States on date 2017-08-04

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Deadline for abstracts/proposals : 1st August 2017

Keynote Speakers : Casper (Cap) Uldriks Former Associate Center Director of FDA's CDRH Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requ

Conference Highlights :Understand FDA's recall authority and policy Learn how to manage recalls under FDA oversight Learn how to interact with FDA See how to develop health risk determinations Learn critical recall strategy components Manage possible FDA enforcement actions

Venue :Salt Lake City, UT, United States

Check the event website for more details.