Instant QMS interpreter
Your QMS was meant to prevent mistakes.Instead, its complexity ensures them.
WHY
Speed and compliance don't mix well.
Every time you sprint, engineers skip the QMS. Delays follow. Audit findings follow. Rework follows.
HOW
Dimando reads your documents and serves instant, cited answers.
Engineers get the right answer before they decide. No rework. No escalations. No audit findings.
WHAT
An instant QMS interpreter.
Ask anything. Get cited answers at the speed of work.
“QMS are hard to navigate. You know it. Your engineers know it. Your auditors know it. And it's very costly every time it goes wrong.”
~15%
of business unit sales lost to a single FDA warning letter remediation
$60M minimum for a $400M unit; up to $500M+ for large divisions.
↗ Compliance Architects30 days
to submit remediation evidence for Grade 4–5 MDSAP non-conformances
Deadline runs from audit end date. Failure prolongs regulatory exposure.
↗ MDSAP Post-Audit Policy (FDA)~0.55%
of annual sales spent on remediation (CAPAs, MDRs, field actions)
Plus ~2.1% more for internal scrap and rework.
↗ McKinsey — Business Case for Medical Device Quality$27,874
per violation for unreported safety defects (NHTSA civil penalty)
Maximum exposure per related series: ~$139M. Updated 2025 figures.
↗ 49 CFR § 578.6 (Law Cornell)60 days
to submit corrective action evidence for major IATF 16949 non-conformances
A special verification audit must follow within 90 calendar days.
↗ IATF Rules 6th Edition (Nov 2024)15–20%
of revenue consumed by total quality costs in complex manufacturing
Internal failures (scrap, rework) are consistently the largest cost driver.
↗ ASQ — Cost of QualityThe same problem. Every role. Every day.
The answers aren't at hand. Mistakes follow.
MedTechVerdant Medical Systems
How it works
Step 1
Connect your QMS
Point Dimando at your existing QMS — PDFs, Confluence, SharePoint. Read-only. Nothing moves, nothing changes.
Step 2
Ask in plain language
Engineers ask questions the way they think them. No boolean queries. No folder navigation. No guessing.
Step 3
Get a cited answer
Every answer references the exact document, section, and revision. Auditable. Trustworthy. Instant.
Before
Turn this
38 documents. One question.
After
Into this
How must my MR be reviewed for a safety requirement?
Safety-tagged merge requests require approval from a peer reviewer AND the Risk Manager before merge. Coverage targets for [SAFETY] units are ≥95% statement coverage.
↳ Found in 1.4 seconds
Before
Turn this
38 documents. One question.
After
Into this
How must my MR be reviewed for a safety requirement?
Safety-tagged merge requests require approval from a peer reviewer AND the Risk Manager before merge. Coverage targets for [SAFETY] units are ≥95% statement coverage.
↳ Found in 1.4 seconds
Turn this
38 documents. One question.
Into this
How must my MR be reviewed for a safety requirement?
Safety-tagged merge requests require approval from a peer reviewer AND the Risk Manager before merge. Coverage targets for [SAFETY] units are ≥95% statement coverage.
↳ Found in 1.4 seconds
Try it out
No signup. No sales call. Type a question, get a cited answer from our sample QMS.
⌘ + Enter to submit
Stop losing answers that are already there.
🇨🇭Swiss partner · 15 years in the market
These brands trust us.
Frequently Asked Questions
- What is Dimando and how does it work?
- Dimando is a QMS navigation tool. It connects read-only to your existing Quality Management System sources — PDFs, Confluence, SharePoint — and answers natural-language questions with citations to the exact document, section, and revision number. No migration, no data upload.
- Which document formats and QMS systems does Dimando support?
- Dimando connects to PDFs, Confluence spaces, SharePoint libraries, and DOORS NG repositories. Your documents remain in your existing systems. Dimando reads them — it never modifies your QMS content.
- How does Dimando keep our QMS documents secure?
- Dimando operates on a read-only basis. It analyzes, maps and serializes your documents in your server, your cloud or external servers. Every answer cites the exact source document and revision so your team can verify results directly. Dimando is designed for ISO 13485 and MDR-regulated environments where data integrity is non-negotiable.
- Which regulatory standards does Dimando cover?
- Dimando is designed for regulated industries including ISO 13485, EU MDR, FDA 21 CFR Part 820, MDSAP, IATF 16949, and ASPICE. Any QMS document your organisation uses can be connected — Dimando does not limit you to a predefined standard library.
- How quickly can a team get started?
- There is no migration, no re-structuring of your QMS, and no training required for engineers. The setup takes 3 to 10 business days depending on your QMS size and complexity.
- What languages does Dimando support?
- Dimando processes documents in the language of your QMS to deliver the highest citation accuracy. Questions and answers can be translated across major languages. Cited source documents are always returned in the original QMS language.