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.
Let Northridge’s risk management experts help you improve your risk management system and find new tools.
We can help you to comply with the latest FDA and European regulations on Computer Systems and Software Validation
Do you need to develop your systems in preparation for audits or in response to new business, the changing regulatory environment or other factors?
We deliver courses in Software and Computer Systems Validation, Risk Management, ISO 14971, Technical Report Writing and more.
“Northridge were instrumental in the Management of our Re-validation programme”