Your RTM.
Done tonight.
A requirements traceability template that works the way you actually work, in a spreadsheet. Free download. Nothing leaves your machine.
How to make audits not suck
Four tabs. One schema.
User Needs, Requirements, Tests, Risks. The relationships that every audit cares about, in a structure your team already knows how to use.
Generate an RTM.
Check your audit status: just drag & drop the file onto RTMify Trace. Get a full analysis and your RTM.
.docx .pdf .md Live traceability updates.
Using RTMify Live: whenever anyone touches a cell in the sheet, every row gets a realtime status update. Gaps surface before the auditor does.
OK NO_TEST_LINKED MISSING_ID How it works
- 1
Download the template
Free .xlsx file. No account, no email, no friction.
- 2
Fill in your requirements, tests, risks
Use the four tabs: User Needs, Requirements, Tests, Risks. Add your IDs, descriptions, and cross-references.
- 3
Drop the file on RTMify Trace
Runs on your machine. No need to call IT, your data always stays local.
- 4
Get an RTM as a PDF / Word Doc / Markdown
Full traceability matrix from requirements to tests to risks. Print it. Email it. Put it in your technical file. Dazzle your friends.
Traceability doesn't need to cost six figures.
Used by quality engineers at medical device, aerospace, and automotive companies. Built by people who've written RTMs at 11pm the night before an audit.
RTMify Live · MCP
"I'm literally talking to my requirements. Jama, Polarion... nobody has this feature."
— RTMify Live user, via Claude Code
Your RTM isn't a static document you update before audits. With RTMify Live, it's a live knowledge graph you can talk to.
See RTMify Live →Standard-specific guidance
The template covers all six standards. Each standards page explains exactly what the standard requires, what the template covers, and where teams typically miss.
AS9100 RTM Template
Aerospace quality management. §8.3 design controls, traceability, and configuration management.
ISO 13485 RTM Template
Medical device QMS. §7.3 design inputs, outputs, V&V, and risk per ISO 14971.
DO-178C RTM Template
Airborne software. HLR/LLR traceability, DAL annotation, bidirectional coverage.
IEC 62304 RTM Template
Medical device software lifecycle. §5.2–5.7, safety class, SOUP tracking.
ISO 26262 RTM Template
Automotive functional safety. HARA, ASIL assignment, V-model traceability.
ASPICE RTM Template
Automotive SPICE. SYS.2/SWE.1–6 bidirectional traceability and capability evidence.
Download the template
Free. No account. No email. Works in Excel and Google Sheets.