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Quality and Certification

  • Establishment and implementation of Quality Systems
  • Preparation for certification of Quality Systems according to FDA QSR, EU Medical Device Directive 93/42/EEC, ISO13485 and CMDCAS.
  • Liaison with certification bodies
  • Pre-certification audits prior to FDA audits, Notified Body Audits or other bodies
  • Periodic compliance audits


 











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