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Reusable Medical Devices – Getting Market Clearance in the United States

 
  April 25, 2016  
     
 
Xtalks Life Science Webinars, Online
2016-05-04


Key Topics will Include:

  • Useful tips for developing validation studies that are accepted on the first submission
  • How to properly classify your device for reprocessing
  • Understanding FDA’s six criteria for reprocessing instructions
  • Understanding cleaning, disinfection, and sterilization – the differences between them and how they should be applied to products based on classification
  • Useful tips on developing Instructions for Use to minimize human error or confusion
 
 
Organized by: Xtalks Life Science Webinars
Invited Speakers: Steven Elliott, Director, Quality Control and Sterility Assurance, NAMSA
 
Deadline for Abstracts: 2016-05-04
 
Registration: Free
E-mail: helpdesk@xtalks.com
 
   
 
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