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Determine Appropriate Field Reporting Processes for Medical Device Corrections and Removals

 
  November 01, 2013  
     
 
Global Compliance Trainings, Online
2014-01-16


·         Areas To Be Covered in this Seminar:


 Food, Drug and Cosmetic Act (The Act) Sections 518(e) and 519(g)

·         21 CFR 810 – Medical Device Recall Authority

·         21 CFR 7 – Enforcement Policy

·         21 CFR 806

·         SG2(PD)/N111R9  guidance document

 

 
 
Organized by: Global Compliance Trainings
Invited Speakers: Mark Perkins 

 

 
Deadline for Abstracts: 2014-01-15
 
Registration: 2013-11-01
E-mail: globalcompliancetrainings1@gmail.com
 
   
 
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