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# medtech

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Jun 28

The 5-Brains Architecture: Engineering a Cyber-Physical T1D Closed-Loop System

#ai #cybersecurity #medtech #architecture

1 min read

Priya Nair

Jun 25

AI for CAPA: fine for "what is it", risky for "is it adequate

#qms #medtech #compliance #regulatory

4 min read

Priya Nair

Jun 25

Management review that isn't a slide show — genuine quality signals

#qms #medtech #compliance

4 min read

James Whitfield

Jun 23

Every eQMS demo looks like electronic forms — which ones actually run workflows?

#qms #medtech #compliance #regulatory

4 min read

Priya Nair

Jun 22

Management review that isn’t a slide show — genuine quality signals

#qms #medtech #compliance

4 min read

Priya Nair

Jun 22

eQMS for EU medtech: practical trade-offs between MasterControl, Greenlight Guru, Qualio, ETQ, Veeva, qmsWrapper

#qms #medtech #compliance

4 min read

Priya Nair

Jun 18

How the IVDR forced me to rethink CAPA — practical changes that actually stuck

#qms #medtech #compliance #regulatory

4 min read

Priya Nair

Jun 16

Annex I §17.2: the cybersecurity checklist I actually use in Technical Files

#qms #medtech #compliance #regulatory

4 min read

Priya Nair

Jun 15

CAPA effectiveness checks — why "closed" rarely equals fixed

#qms #medtech #compliance

4 min read

Priya Nair

Jun 10

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

#qms #medtech #compliance

4 min read

Priya Nair

Jun 4

AI can explain CAPA — but it cannot certify adequacy (here’s how I use it)

#qms #medtech #compliance #regulatory

4 min read

James Whitfield

Jun 3

CE marking under MDR — what's actually new vs what teams keep getting wrong

#qms #medtech #regulatory

3 min read

Priya Nair

Jun 1

Near-misses vs device failures — what MAUDE actually tells a European RA

#qms #medtech #compliance

4 min read

Priya Nair

Jun 1

MDR reform proposals (Dec 2025) — what the breakthrough pathways actually mean for manufacturers

#medtech #regulatory #compliance

4 min read

Priya Nair

May 29

How I validate LLMs for GxP work — scope, evidence, and the auditor's checklist

#qms #medtech #compliance #regulatory

4 min read

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