Today, we're publishing our 30-page EU MDR Roadmap, worth hundreds (thousands?) of Euros, for free.
What's the Roadmap? Think of it like a (very) long to-do list which contains all the detailed steps you need to go through if you want to bring a medical device to market in the EU. This is the blueprint of our work as consultants - it's the process we've been following for the past 5 years, during which we successfully helped 150+ companies with their medical device compliance and passed countless audits.
This is all our knowledge as consultants, condensed into one PDF.
In the past, we’d only provide this Roadmap to our consulting clients - companies who would pay us thousands of Euros to help them with their compliance documentation. And that was cool, because we were usually still 50%+ cheaper than other consultants.
But now, things are changing.
With ChatGPT and LLMs, I don’t think you’ll really need a whole lot of consulting any more. Just ask ChatGPT. Sure, ping us if you have questions, especially when it comes to what really works in audits. But we'll no longer be selling expensive consulting to you. We've put everything you need to know out there already, for free: Our free templates, free articles, free community, and our free YouTube channel.
If you want to get your medical device compliance done yourself, you now have all the resources you need.
And if that means that, some day, we’ll be shutting down our consulting business, I’m all for it! Any sort of consulting activity is an indication that not enough information is freely available in a given field. We’re here to change the field of medical device compliance, and we’re here to make more information freely available.
This PDF Roadmap is another example of that.
But don't worry - we’ll still be around :)
With more information freely available, the next-highest leverage for you and your company to get your medical device compliance done (fast!) is to use an eQMS software which helps you automate as much as possible.
And we’ve been working hard on building just that.
Check out Formwork, the most affordable eQMS for agile, lean, founder-led companies. On the market for 5 years, used by thousands of companies. It has passed EU MDR, FDA and Health Canada audits.
While ChatGPT and publishing all our knowledge will hopefully make consulting go away, we'll be hard at work providing you with the best (and most affordable) software to manage and optimize your regulatory documentation going forward.
All the best with your medical device compliance :)
Ah right.. almost forgot the link. Here you go: EU MDR Roadmap - PDF download, no strings attached, we don't gather your email, etc., etc. - you know us :)
What's the Roadmap? Think of it like a (very) long to-do list which contains all the detailed steps you need to go through if you want to bring a medical device to market in the EU. This is the blueprint of our work as consultants - it's the process we've been following for the past 5 years, during which we successfully helped 150+ companies with their medical device compliance and passed countless audits.
This is all our knowledge as consultants, condensed into one PDF.
In the past, we’d only provide this Roadmap to our consulting clients - companies who would pay us thousands of Euros to help them with their compliance documentation. And that was cool, because we were usually still 50%+ cheaper than other consultants.
But now, things are changing.
With ChatGPT and LLMs, I don’t think you’ll really need a whole lot of consulting any more. Just ask ChatGPT. Sure, ping us if you have questions, especially when it comes to what really works in audits. But we'll no longer be selling expensive consulting to you. We've put everything you need to know out there already, for free: Our free templates, free articles, free community, and our free YouTube channel.
If you want to get your medical device compliance done yourself, you now have all the resources you need.
And if that means that, some day, we’ll be shutting down our consulting business, I’m all for it! Any sort of consulting activity is an indication that not enough information is freely available in a given field. We’re here to change the field of medical device compliance, and we’re here to make more information freely available.
This PDF Roadmap is another example of that.
But don't worry - we’ll still be around :)
With more information freely available, the next-highest leverage for you and your company to get your medical device compliance done (fast!) is to use an eQMS software which helps you automate as much as possible.
And we’ve been working hard on building just that.
Check out Formwork, the most affordable eQMS for agile, lean, founder-led companies. On the market for 5 years, used by thousands of companies. It has passed EU MDR, FDA and Health Canada audits.
While ChatGPT and publishing all our knowledge will hopefully make consulting go away, we'll be hard at work providing you with the best (and most affordable) software to manage and optimize your regulatory documentation going forward.
All the best with your medical device compliance :)
Ah right.. almost forgot the link. Here you go: EU MDR Roadmap - PDF download, no strings attached, we don't gather your email, etc., etc. - you know us :)
