Get Notified About Regulatory Updates
Dr. Oliver Eidel
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Formwork Features
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Updated May 19, 2024
In the past, learning about regulatory updates for staying up to date with medical device standards like the ISO 13485, IEC 62304 and others has either been very clunky or rather expensive.
Today, we're launching Regulatory Updates in our eQMS software, Formwork, and the best thing is that we're making it available to everyone, for free!
There's literally no reason not to use it - it'll save you lots of time, help you pass your audits and it's free.
Check out Formwork here and sign up for a free account :)
Today, we're launching Regulatory Updates in our eQMS software, Formwork, and the best thing is that we're making it available to everyone, for free!
There's literally no reason not to use it - it'll save you lots of time, help you pass your audits and it's free.
Check out Formwork here and sign up for a free account :)
On a different note: Do you need any help with your EU MDR efforts?
We’ve worked with 100+ companies and helped them certify their devices in weeks, not months. Talk to us now – first calls are free! Check out our services and prices here.
Or, if you don’t like talking to humans, check out our Wizard. It’s a foolproof, step-by-step video course for getting your compliance done yourself.
And if you’re looking for the best QMS software for lean, founder-led companies, check out Formwork. It automates your compliance, and there’s even a free version for you to try out!
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Dr. Oliver Eidel
I’m a medical doctor, software engineer and regulatory dude. I’m also the founder of OpenRegulatory.
Through OpenRegulatory, I’ve helped 100+ companies with their medical device compliance. While it’s also my job that we stay profitable, I try to dedicate a lot of my time towards writing free content like our articles and templates. Maybe that will make consulting unnecessary some day? :)
If you’re still lost and have further questions, reach out any time!
Through OpenRegulatory, I’ve helped 100+ companies with their medical device compliance. While it’s also my job that we stay profitable, I try to dedicate a lot of my time towards writing free content like our articles and templates. Maybe that will make consulting unnecessary some day? :)
If you’re still lost and have further questions, reach out any time!