Northridge Quality
& Validation

Validation and Quality Management for the Medical Device Industry

Northridge Quality & Validation provides quality management consultancy to the Medical Devices Industry in the areas of Risk Management, Validation and Quality Systems.

Our mission is to save Life Sciences companies time and money by carrying out projects in a timely fashion whilst keeping client resource requirements to a minimum.

Risk
Management

Let Northridge’s risk management experts help you improve your risk management system and find new tools.
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Software
Validation

We can help you to comply with the latest FDA and European regulations on Computer Systems and Software Validation
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Process
Validation

Let us streamline your validation process
to ensure that you are getting the most out of your process.
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Quality Systems

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

We deliver courses in Software and Computer Systems Validation, Risk Management, ISO 14971, Technical Report Writing and more.
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auditing

AUDITING

Whether it be a Customer, FDA, Notified Body/ Regulatory Body Audit your team can benefit greatly from our experienced personnel's help.
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“Northridge were instrumental in the Management of our Re-validation programme”
Justin Walsh
Plant Manager, Boston Scientific, Letterkenny.