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.

Built for medical device teams

Early access is open to quality and regulatory teams

MEDDEV structured

Follows the 2.7/1 Rev. 4 review structure

48% less time

Internal testing, three client projects

Three teams

Using it on live projects

Early access

Open to a small number of teams

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

Measured in internal testing

What we have measured so far

SOTA Navigator is in private beta. This is what internal testing showed, and the workflow that produced it.

48%
Less time per review

Measured in internal testing across three client projects

PICO
Questions built first

PICO tables are a step in the workflow, before any query runs

PRISMA
Counts that reconcile

Every count recorded as you screen, not reassembled at the end

Beta
Private programme

Open to a small number of teams while we build alongside them

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.

48% less time per review

Measured in internal testing across three client projects. The saving comes from the screening and deduplication steps, which is where the repetitive work sits.

The search you can run again

Search strings are stored verbatim, so the update is the same query against a new date range instead of a fresh search that happens to look similar.

Structured the way the guidance is

The workflow follows the MEDDEV 2.7/1 Rev. 4 literature review structure, from PICO tables through screening and appraisal to the PRISMA flow.

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