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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
Venue
online

online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States

Organised by
Global Compliance Trainings
Contact information
john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, Suite 1007,, Auburn Hills,, michigan., 48326, United States of America
2482120588
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