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One NCR form to rule them all stopped working the day we added our 30th supplier

Last month, a buyer pinged me: "Why is this incoming-inspection NCR asking me whether the customer filed a complaint?" Fair question. It's because w…

qmsmedtechcompliancetesting
Dev.to Oct 14, 2026, 09:29 UTC
EN

The AI approval boundary nobody talks about until the audit finds it

The first time I saw an AI approve a CAPA closure, I'll admit I paused. Not because the decision was wrong — it wasn't — but because I couldn't find…

qmsmedtechcomplianceregulatory
Dev.to Sep 11, 2026, 02:01 UTC
EN

Begin with control; the real win is turning it into daily practice

To be fair, "we have a QMS" is the easiest checkbox in a notified‑body audit. The hard part is that regulators, auditors and — most importantly — fr…

qmsmedtechcompliance
Dev.to Aug 31, 2026, 14:05 UTC
EN

The cleanest way to keep your compliance‑AI out of the EU AI Act high‑risk class: AI proposes, a human approves and signs

I nearly signed off on an "auto‑close" feature for an AI that triaged evidence requests. It would have saved the team hours a week. We didn't enable…

qmscomplianceregulatory
Dev.to Aug 25, 2026, 10:14 UTC
EN

Picking an eQMS for a 200-person Class II device shop — a pragmatic comparison

I work in a 200-person Class II medical device company with two QA/RA folks, three embedded-hardware teams, a small supplier-quality group, and engi…

qmsmedtechcomplianceregulatory
Dev.to Aug 22, 2026, 15:11 UTC
EN

Traceability matrices die when treated as documents — how to keep traceability living

I used to maintain a traceability matrix as a 30‑row table in a Word document. It looked tidy on a submission day and then rotted quietly for the ne…

qmsmedtechcompliance
Dev.to Jul 19, 2026, 14:51 UTC
EN

Where usability files actually break — and what I do about it

I stopped treating the usability file as a compliance artifact years ago — it’s where product design and real people collide. When it’s done badly,…

qmsmedtechcomplianceregulatory
Dev.to Jul 13, 2026, 19:06 UTC
EN

Picking an eQMS for an EU medtech SME — practical pros and cons of six vendors

I support CE-marked Class IIa/IIb devices under MDR every week. Choosing an eQMS is rarely a technology decision alone — it’s a systems, audit-readi…

qmsmedtechcompliance
Dev.to Jun 10, 2026, 14:12 UTC
EN

Why our eQMS ran in parallel for 18 months — and what I’d do differently

I’ve been responsible for maintaining a Class II product’s QMS during one of the messiest migrations I’ve seen: an 18‑month parallel run where the o…

qmsmedtechcompliance
Dev.to May 19, 2026, 22:20 UTC

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