Special Processes Made Simple: What Aerospace and Medical Device Standards Are Actually Asking For
Introduction In the aerospace and medical device manufacturing industries, there exist select processes that cannot be…
The Deadline Ledger: The Coming Wave of Quality Standard Transitions
Introduction Change doesn’t come overnight in quality management systems. The material that shepherds auditors and…
How AS9101 and AS9104 Changed AS9100 Audits: A Retrospective
With the new revisions in effect for AS9101 and AS9104 by the International Aerospace Quality Group (IAQG), the world…
What You Need to Know About Getting Certified in AS9100: Timelines, Salaries, and the Future
"AS9100 is as lucrative as it is regulated." Introduction When prospecting quality assurance in the aerospace and…
Breaking Down the Latest IA9100 Updates- What You Need to Know Now
What’s Going On with AS9100? If you've been scrambling to learn more about the next update to AS9100 and what it might…
What AS9100 Means by “Critical Items” and Why You Need to Define Them
Have you ever scanned through AS9100 Clause 8.1.1 and scratched your head at the mention of “critical items”? If so,…
Product Safety in AS9100: What It Actually Means, and What You’ll Need to Show
A Comprehensive Walkthrough of One of The Most Important Facets of Aerospace Manufacturing Product safety isn’t a new…
Duality of Posterity: A Review of AS9100’s “Documented Information”
The Paper Trails of QMS Made Simple If a strong process exists without any documentation, is it really a strong…