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Technical Writing Tip of the Month - The Description
8th April 2021

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


Validation and Quality Management for the
Pharmaceutical and Medical Device Industries

Northridge Quality and Validation provides services to the Medical Devices and Pharmaceutical Industries in the areas of Validation, Risk Management, Quality Systems, Health and Safety and Environmental Management.

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.

We carry out practical projects, working alone or in conjunction with client staff as well as providing training and technical advice. Our personnel are specifically chosen to suit your project so that you get the experience and knowledge required for successful project completion.

Transferring knowledge to the client to allow them to become self sufficient is a core value at Northridge.

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Looking for Validation Engineers?
Northridge Pioneers in-house Validation Staff Upskilling programme.

Northridge Quality and Validation has pioneered a new, customer centric approach to the coaching of staff responsible for the maintenance of validation documents.

Finding it hard to source validation engineers? Looking for qualified, professional validation specialists? Why not upskill some of your current personnel to take on this vital role instead? With Northridge's new in-house coaching programme, you can turn members of your trusted staff into competent validation technicians.

We coach Technicians, Quality Personnel, Managers, Team Leaders etc from other Departments in-house to complete validation documents to FDA and European regulation standards. Your staff will learn the skills to complete validation and risk management activities without having to leave the workplace and your validations will progress as they learn.

The programme will be tailored exactly to your requirements and will cover the validation documents required by your system, such as; Change Control Notices, VMP, Risk Management Plans, FMEA, URS, FDS, IQ, OQ & PQ Protocols and Reports and Trace Matrices. One of our validation experts will come on site to train your staff to your procedures and bring them through the full validation documentation gambit, with follow up available as required on an ongoing basis. Groups of six, to as few as one, can be catered for and the timing can be tailored around your staff's work demands. At the end of the programme, you will end up with trained validation technicians staff and completed validation packages.

John Lafferty, Northridge's MD says, "this service grew from customer's requests to us - utilizing valued members of staff who know the company and the business can prove an excellent alternative to recruiting temporary validation staff or contractors when it comes to completion of mission critical validation programmes"

Contact us for a free consultation now
or call us on 00353 87 2801793.

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