All things CAPA in IS0-9001 standards
Every organization has its share of problems; customer complaints, process defects, faulty components, misleading data or reports, and a plethora of […]
A Comprehensive Guide to Non-Conformance Management
What is a Non-Conformance report? Simply put, it is a report or document detailing the failings or shortcomings of a
Calibration: The Definitive Guide about Calibration
Calibration is the act of confirming that a method or system, or instrument used in measurement will produce correct results.
Document Control: Step-by-Step Guide 2022
In general, Document Control is a profession and a job role. It is now universally implemented in various activity sectors. It is
ISO and Document Control (ISO 9001:2015)
What is document control as it relates to ISO requirements? Document Control is a document management operation whose purpose is to enforce controlled processes and
A Brief History of Document Control
Ever since man first scratched an idea in the dirt, it became evident that a process to document the idea,
Key Concepts in Understanding The Quality Management
The following content is offered to our readers as a short list of important concepts, principles and definitions that can
IT’S ALL ABOUT RISK (Part 1) ISO 9001
Background Somebody finally got it right…Quality and Quality Systems is all about avoiding risks. Meeting requirements, delighting customers, and other
Dangers in Poor Corrective Action Systems
A poor corrective action system can pose significant risks to an organization, hindering its ability to effectively address issues and
ISO 9001 – Tyrant or Servant (Part 1)
(Part 1 of a 3-part series) Background Most small to medium size companies implement an ISO 9001 based Quality Management System (QMS)