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What is the difference between the EN and ISO versions of 14971:2019? Part 1
14th September 2020

What is the difference between the EN and ISO versions of 14971:2019? Part 2
14th September 2020

Is Analysis of Multiple-Fault Conditions a Requirement of ISO14971?
14th September 2020

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Quality Systems

Could you use some extra resources to run your Quality Systems?

Do you need to develop your systems in preparation for audits or in response to new business or the changing regulatory environment?

Our highly qualified, experienced personnel can help you with the following processes:

  • Complaint Handling
  • CAPA
  • CE Marking/510Ks
  • Regulatory Filings
  • Audit Preparation
  • Internal Auditing
  • Supplier Auditing
  • Quality System Development
  • Changes to comply with new standards or regulations
  • GMP Training

    Are you a supplier to the life sciences industry?

    Northridge can help you to comply with the following regulations:

  • GMPs
  • ISO 13485
  • US FDA QSR Parts 211 & 820


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