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Technical Writing Tip of the Month - Key Elements of a Good Document
4th February 2020

Update on Three Medical Device-Related ISO Standards
19th December 2019

ISO 14971:2019 has been just been published!
11th December 2019


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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