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Determine Appropriate Field Reporting Processes for Medical Device Corrections and Removals

30 May 2014, michigan., United States


Introduction
A review of the relevant sections of the Food, Drug and Cosmetic Act and sections of 21 CFR that FDA utilizes to regulate either the initiation and/or reporting of Medical Device Corrections and Removals, and an overview of status of SG2(PD)/N111R9 guidance document in process to address global harmonization
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online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States

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Global Compliance Trainings
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