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Free online check for medical device developers

MedTech Compass.
Know what to do first.

In 10 minutes, see your likely regulatory path, your biggest gaps, and your next priorities so you know what to fix first and what can wait.

Three steps that show where your time is best invested right now.

Regulatory scope

  1. Intended purpose

  2. MDR classification

  3. Clinical evaluation

  4. Risk management

  5. ISO 13485

  6. CE marking

For software and traditional medical devices.

Why founders get stuck

Regulatory information is everywhere. Clear direction is harder to find.

Most guidance is written in general terms, which makes it difficult to know what applies to your product, your stage, and your market goals.

MedTech Compass filters the noise and turns your answers into a clear priority list: what matters now, what can wait, and what to look at next.

How it works

From product profile to next steps in about ten minutes

MedTech Compass asks a guided set of questions about your product, development stage, target markets, and what you have already completed.

Based on your answers, it gives you a structured first view of your likely regulatory path, key gaps, and next priorities.

It is not a full roadmap to approval. It is a clear starting point — so you can see where you stand, what matters now, and what to do next.

The check takes about ten minutes. Your result appears immediately after you submit your name and email address.

  1. 01

    Capture the product profile

    Category, development stage and target markets.

  2. 02

    Compare against the open requirements

    Your inputs, checked against what still needs to be in place.

  3. 03

    Prioritised next steps

    A short, ordered list specific to your product.

Fit

Is MedTech Compass right for you?

A good fit

MedTech Compass is built for founders developing a medical device who know regulation is coming, but do not yet have a clear plan.

It works at any stage: early idea, product development, investor preparation, or approval planning. The earlier you use it, the easier it is to see what matters before decisions become harder to change.

Less suited

MedTech Compass is less useful for experienced teams that have already taken several products through approval and already know their regulatory path.

If that sounds like you, expert validation or hands-on regulatory support may be a better next step.

Get Started

Get Started

MedTech Compass gives you a product-specific view of where you stand, what matters now, and what to do next in about ten minutes.

Start the compass

The result appears immediately after you enter your name and email address.