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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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Process Validation

Efficient Effective Validation

We have engineers, chemists and other specialist personnel available who can carry out any part of your validation project from:

  • Validation Plans
  • Validation Risk Assessment
  • Writing of Validation Plans
  • IQ OQ and PQ protocols
  • Running of Validation Trials
  • Product Testing
  • Writing Validation Reports.

    We can supply you with personnel who are fully experienced in the latest techniques in process validation. Our personnel are experienced in;

  • Design of Experiments
  • Application of Sampling Plans
  • Test Method Validation

    By using Northridge to assist in your validation process you can bring process improvements to fruition faster, making sure that you reap the benefits of those improvement at the earliest possible time.

    Streamlining the Validation System

    Is your validation system as lean and effective as it could be? Let us streamline your validation process to ensure that you are getting the maximum benefit for the minimum of effort. We can help you save time and valuable resources by ensuring that validations are successful first time. We streamline validation by optimising sampling plans to ensure that all validation testing adds value and by ensuring that validation protocols and reports are written efficiently.


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