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NAMSA evaluates safety for medical devices in four phases. This approach is designed to ensure regulatory compliance and get your product to market quickly.
Research and Development Design Manufacturing Quality Assurance

  • Characterization of Materials
  • Function & Performance Testing
  
  • Biocompatibility of Materials
  • European Clinical Trials
  
  • Environmental Control
  • Manufacturing Process Control
  • Sterility
  • Finished Product Qualification

  
  • Release Testing   
  • Periodic Audit Testing  
  
 



 



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