How Supplier Quality Audits Drive Zero Defect Manufacturing

How Supplier Quality Audits Drive Zero Defect Manufacturing

The concept of “zero ppm” (parts per million) or “zero defects” has been around since the[…]

Unlocking Business Excellence: A Guide to ISO 9001 and Internal Audits

Unlocking Business Excellence: A Guide to ISO 9001 and Internal Audits

Over a million organizations worldwide trust the ISO 9001 Quality Management System (QMS) to achieve consistent[…]

Regulatory Changes in the Automotive Industry in 2024

Regulatory Changes in the Automotive Industry in 2024

As you may already know, IATF 16949 is one of the most widely used standards for[…]

The Power of Engagement: How a Proactive QA Team Conquers Nonconformances and CAPAs

The Power of Engagement: How a Proactive QA Team Conquers Nonconformances and CAPAs

In the world of manufacturing, quality is everything. Even minor deviations from specifications, known as nonconformances,[…]

Understanding Deviations (Issues) in Manufacturing: The Second Class of Non-Conformances

Understanding Deviations (Issues) in Manufacturing: The Second Class of Non-Conformances

In the relentless pursuit of quality, manufacturing thrives on consistency and adherence to specifications. However, even[…]

In-depth on CFR 11

In-depth on CFR 11

The U.S. Food and Drug Administration (FDA) plays a vital role in protecting public health by[…]