Northridge Quality
& Validation Ltd

Validation and Quality Training for the Medical Device Industry through our training partner

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

Our mission is to be a training partner for Life Sciences companies. We seek to make a significant and measurable contribution to the organisations we work with. We provide our courses via our training partner, SQT Training Ltd.

Risk
Management

Our Risk Management course provides attendees with the skills they need to comply with ISO 14971:2019 and Medical Device Regulations with a focus on implementation.
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Software
Validation

Our interactive Software Validation training provides attendees with the knowledge they need to comply with European, US and Worldwide software validation requirements.
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Process
Validation

Our Process and Equipment Validation course equips attendees with the skills and knowledge required to comply with European, US and Worldwide validation requirements.
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Technical Writing Skills

Having trouble writing reports, procedures, or other documents? Attending our comprehensive training course will help you to communicate clearly and save you time.
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MDSAP

This course details the main requirements of the regulations from Brazil, Australia, Canada and Japan and shows how these relate to ISO 13485: 2016 and the US QSR and how to audit against them.
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auditing

CAPA

This Corrective and Preventive Action (CAPA) course provides attendees with all the knowledge they need to comply with the CAPA-related requirements of ISO 13485 and 21 CFR Part 820.
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