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✦ AI-Powered Regulatory Intelligence

Regulatory complexity, simplified.

NAVJUN transforms how product teams navigate regulatory requirements. Get instant, accurate answers to complex compliance questions — with full source citations and privacy by design.

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NAVJUN Assistant
What are the MDR Article 10 requirements for a Class IIb device?
Under MDR Article 10, Class IIb manufacturers must establish a post-market surveillance system, maintain a technical file with clinical evaluation (Annex XIV), and appoint an authorised representative if outside the EU. — MDR 2017/745, Art. 10 ¶1–15

80%

Faster research

99%

Citation accuracy

Built for the teams that can't afford to get compliance wrong

From MDR to FDA 510(k), NAVJUN delivers instant, cited answers so your team moves faster with full confidence.

80%

Save Time

Cut research time from hours to minutes. NAVJUN delivers cited regulatory answers instantly, right when your team needs them.

99%

Increase Confidence

Every answer cites the exact regulation, article, and paragraph. Never second-guess a compliance decision again.

40%

Accelerate Development

Shorten regulatory review cycles and reduce costly back-and-forth with notified bodies and regulatory affairs teams.

100%

Maintain Privacy

Your data never leaves your control. Zero-knowledge architecture ensures your IP and regulatory strategy stay private by default.

100+
Regulatory frameworks covered
< 5s
Average response time
99.9%
Source citation accuracy
0
Customer data stored on our servers

Security by design, privacy by default.

NAVJUN is built on a zero-knowledge architecture. Your regulatory queries, documents, and IP never touch our servers. We process everything client-side with end-to-end encryption.

🔒 End-to-End Encrypted
✅ SOC 2 Type II
🇪🇺 GDPR Compliant
🏥 HIPAA Ready
Zero-Knowledge Architecture

Your data is encrypted before it leaves your device. NAVJUN never sees your queries or documents — only you have the keys.

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From question to compliance in three steps

NAVJUN delivers regulatory answers in seconds. Simply ask, verify, and move forward with confidence.

1
STEP 01

Ask your compliance question

Type any regulatory question in plain language. NAVJUN understands product context and target market to deliver the most relevant answer.

2
STEP 02

Get cited, verified answers

Receive a precise answer with citations to the exact regulation, article, and paragraph -- traceable and audit-ready.

3
STEP 03

Move forward with confidence

Export your compliance rationale and integrate it into your documentation workflow. No second-guessing required.

Built for every team that touches compliance

Whether you're designing, building, or certifying — NAVJUN gives your team instant regulatory clarity at every stage.

Product Designers

Navigate MDR, FDA, and CE requirements without becoming a regulatory expert. Get cited answers in seconds, right in your workflow.

01

R&D Engineers

Get instant compliance answers during design sprints — not weeks later from a consultant. Ship faster with fewer regulatory surprises.

02

Regulatory Affairs Teams

Stop manual research. NAVJUN surfaces the exact regulations you need and helps draft compliance rationale — fully cited, audit-ready.

03

Quality & RA Managers

Own your audit trail from day one. NAVJUN generates traceable, regulation-linked documentation your notified body will trust.

04

Ready to transform your product compliance?

Join forward-thinking product teams who've made regulatory complexity a competitive advantage. Start free, no credit card required.