Break Free from Manual Literature Reviews

Your Team Deserves Better Than Endless Excel Sheets

Transform your literature review process from weeks to days. Our smart automation helps medical device teams ensure compliance while saving valuable time.

Trusted by Medical Device Teams

Early access program now open for quality and regulatory teams

MDR Ready

Built for regulatory compliance

2x Faster

Initial testing results

10+ Teams

In beta program

Early Access

Limited spots available

Stop Wasting Time on Manual Literature Reviews

Your team is too valuable to waste time on manual data entry and Excel sheets. See how SOTA Navigator transforms your workflow.

No More Excel Chaos

Automated data extraction saves 40+ hours per review

Smart Search & Analysis

Find relevant papers in seconds, not hours

Guaranteed Compliance

Built-in MDR compliance checks eliminate errors

Add here a screenshot of the SOTA Navigator dashboard

50h+

Saved/Review

Early Results Show Promise

See how our early adopters are transforming their review process

0+
Hours Saved Per Review

Based on initial testing

0+
Articles Analyzed

In our beta program

0+
Reviews Completed

With early adopters

2x

Faster Reviews

Average improvement

Proven Results for Medical Device Teams

Real Results, Real Impact

See how SOTA Navigator is transforming literature reviews for medical device companies worldwide

85%
Time Saved

Average reduction in review time

20+
Hours Saved

Per literature review

25%
Cost Reduction

In review process expenses

10+
Active Teams

In our beta program

Everything You Need, Nothing You Don't

Purpose-built for medical device teams, with features that actually make your life easier.

One-Click PRISMA

Generate perfect PRISMA flowcharts instantly. No more manual diagrams or formatting headaches.

Fits Your Process

Adapts to your SOPs, not the other way around. Custom workflows that match your needs exactly.

Built-in Compliance

Every feature designed for MDR compliance. Pass audits with confidence every time.

Real-time Insights

Track progress, spot trends, and make decisions faster with automated analytics.

Built for Medical Device Teams

Validated for Medical Device Excellence

Meeting the highest standards for medical device development and compliance

ISO 14971 Compliant

Aligned with medical device risk management standards

FDA 21 CFR Part 11

Electronic records and signatures compliance

ISO 13485 Ready

Supporting quality management system requirements

Regulatory Ready

Built for medical device submission requirements

The Impact on Your Bottom Line

Calculate how much time and money you could save with SOTA Navigator.

Save 20h Per Review

Complete in hours what used to take weeks. Automated workflows eliminate repetitive tasks.

90% Less Manual Work

Free your team from data entry. Focus on analysis and strategic decisions instead.

Zero Compliance Risks

Eliminate the cost of non-compliance. Every review meets MDR standards automatically.

Client Success Stories

What Our Clients Say

Trusted by leading medical device companies worldwide

"SOTA Navigator has transformed our literature review process. What used to take weeks now takes days, with better accuracy."

D
Dr. Sarah Chen
Medical Device Regulatory Lead
MedTech Innovations

"The automated screening and data extraction features have significantly improved our systematic review workflow."

J
James Wilson
Research Director
BioMed Solutions

"Outstanding compliance features. Makes regulatory submissions so much more manageable and reliable."

D
Dr. Maria Rodriguez
Quality Assurance Manager
DeviceCare Global
4.9/5 average rating from our clients

Common Questions

Everything you need to know about transforming your literature review process.

Get Started Today

Ready to Transform Your Literature Review Process?

Join leading medical device companies using SOTA Navigator to streamline their research

No credit card required • Free consultation • Live demo with our experts