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    FDA Recalls - Before You Start, and After You Finish

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    Website https://www.complianceonline.com/fda-recall-program-training-workshop-seminar-training-80331SEM-prds | Edit Freely

    Category

    Deadline: September 28, 2020 | Date: October 08, 2020-October 09, 2020

    Venue/Country: Washington, D.C, U.S.A

    Updated: 2020-04-05 03:45:00 (GMT+9)

    Call For Papers - CFP

    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 history of recalls. Reiterative recalls lead the FDA to the conclusion that, "You don't get it."

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.