ISO 13485 Medical Device QMS Starter
Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Home / Medical / Medical Device Cybersecurity Documentation Kit (FD&C Act 524B)

Threat model, exploitability-based risk assessment, SBOM inventory, vulnerability log and submission checklist. Not regulatory advice.
$77
Buy on Payhip · $77Secure checkout by Payhip. Download link by email right after purchase.
See sample pages (PDF preview)
Small medical device makers, startups and contract manufacturers building or tightening an ISO 13485 / FDA quality system.
Pay through Payhip and you get a download link on screen and by email. Files open in Microsoft Office, Google Docs/Sheets and LibreOffice.
Questions? Support
Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Gap assessment mapping the old QSR to the QMSR / ISO 13485, a records matrix and a transition plan. Templates, not regulatory advice.
What's inside →Risk plan, hazard analysis tied to an editable acceptability matrix, FMEA, benefit-risk and the risk management report. Templates, not regulatory advice.
What's inside →