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Blog
Are you ISO 14971:2012 compliant? Understanding Content Deviations
3rd September 2019

Technical Writing Tip of the Month - Understand your Audience
30th August 2019

ISO 14971: 2012 Compliance Content Deviations #1 and #2: Treatment of Negligible Risks and Risk Acceptabililty
1st August 2019

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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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