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Determine Appropriate Field Reporting Processes for Medical Device Corrections & Removals

Posted on May 28, 2014 3:27:00 PM

 

Conference - Online

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 harmonizationSpeaker: Jerry Dalfors

Organization: Global Compliance Trainings

For more information, please visit: http://www.globalcompliancetrainings.com/index.php?route=product/product&product_id=18&list=Jerry%20Dalfors

May 25, 2014 - May 25, 2014 (10:00AM - 01:00PM)

201, N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326

 Contact: John Gordan (webinar@globalcompliancetrainings.com)

Phone: 2482120588

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Tags: 2014, Medical Device Technology, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

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