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In this webinar we discussed...

  • Regulatory aspect as per ISO 13485 & 21 CFR part 820.30
  • Important aspects to be taken care during design and development
  • Stages and steps of the medical device development
  • The interrelationship between risk assessment, usability engineering with design and development.
  • Question and Answer session

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Our Services

Manufacturing Site Design and Conceptualization

Medical Device Certification and QMS

Medical Device/Drug-Device Combination Product Design & Development

Medical Device Post Marketing Support