Human Error or a Bigger Problem? When to Dig Deeper
by Julius DeSilva In the world of process improvement and problem-solving, human “user” error can often become the
ISO 13485: QMS Requirements of Medical Devices for Regulatory Purposes
by Dr. IJ Arora ISO 13485:2016 is a standard that addresses quality management system requirements for those within
One-Off or Systemic: The Search for Root Causes
by Julius DeSilva Accidents and failures, whether in maritime, aviation, healthcare, or nuclear settings, are often subjected to
QMII Webinar Topic – Creating Meaningful Audit Checklist
QMII recently conducted a webinar on the topic “Creating Meaningful Audit Checklist” which was presented by CEO –
The Role of Management Systems in the Tragic Collision Over the Potomac
by Dr. IJ Arora A significant tragedy occurred in Washington D.C. on January 29, 2025, with the deadly
Are Provider Audits Mandated through ISO 9001?
by- Dr. IJ Arora In relation to outsourced processes, the query (to paraphrase William Shakespeare) is, “To audit
Writing of ISO Requirements? ISO 21973:2020
In this article the author makes a case for a harmonized approach to writing ISO standards to make integration easier as also changes that would benefit users of ISO 21973
Leadership and Strategy: ISO 9001 & ISO 22000 Executive Overview
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QMII Webinar – Proactive Internal Auditing
Offered via Julius DeSilva Click on right here for the presentation
The Role of Shipowners in Ensuring MLC Compliance
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