Radiation Sterilization of Medical Products - Beyond the Basics 2017

  • 23-24 May 2017
  • Sheraton Mahwah Hotel, NJ, United States

Description

Topics
  • How to complete an optimal validation test design inclusive of dose, dosimetry, sample size, accelerated ageing, ASTM standards, and thermal analysis
  • How to select product polymer materials for optimal product performance after radiation sterilization processing
  • All the foundations of a successful radiation sterilization program materials, bioburden, validation, maintenance of validation
  • The effect of product design and assembly on bioburden, product safety and the success in executing the validation journey
  • Perform risk assessments effectively
  • The impacts of all regulatory guidances on the radiation sterilization process
  • Where companies miss the mark in triggering, investigating and executing bioburden action levels and quarterly sterilization audits
Who should Attend
  • Sterilization managers
  • Senior quality managers
  • Regulatory and Compliance professionals
  • Quality professionals
  • Manufacturing engineers
  • Production supervisors
  • R&D engineers
  • Production engineers
  • Quality engineers
  • Process owners
  • Medical affairs
  • Quality auditors
  • Legal professionals

Past Events

Important

Please, check "Radiation Sterilization of Medical Products - Beyond the Basics" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical laboratories, Medical technology, Pharma

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