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ISO 9001 audit readiness: a step-by-step guide and checklist for regulated manufacturers

ISO 9001 audit readiness: a step-by-step guide and checklist for regulated manufacturers

by Bethan Vincent | Aug 25, 2026 | Insights

Preparing for an ISO 9001 audit comes down to four key things:  Keeping your documented information current and under control Showing that your processes run the way you say they do Closing out open nonconformities before the auditor arrives  Rehearsing the whole...
Horizons: From barely visible to ISO 9001 audit-ready

Horizons: From barely visible to ISO 9001 audit-ready

by Bethan Vincent | Aug 25, 2026 | Case Studies

About the client Horizons Incorporated designs, manufactures and installs high-value product identification and asset tracking nameplates, labels and control panels that automate maintenance, inspections, compliance and other business functions.  It serves customers...
Spreadsheets vs SharePoint vs QMS Software: What’s best for regulated manufacturing

Spreadsheets vs SharePoint vs QMS Software: What’s best for regulated manufacturing

by Bethan Vincent | Jul 21, 2026 | Insights

The short answer Spreadsheets and SharePoint both control documents well enough until you are audited against a standard like ISO 9001 or FDA 21 CFR Part 11. At that point you likely do need a software system to handle the complexity.  A dedicated quality management...
How Quality Management Systems Power TQM in Manufacturing 

How Quality Management Systems Power TQM in Manufacturing 

by Ben Jones | May 6, 2026 | Insights

by Tom Rootes, Group Strategic Programmes Director In heavily regulated industries like aerospace and automotive, mid-sized manufacturers face the dual challenge of maintaining strict compliance while striving for continuous improvement. At the heart of these demands...
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