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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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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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