Stay Ahead of a rapidly evolving market and competition, and leverage resources and time

 “I first heard of MedBoard via TOPRA, and since subscribing have found it to be an extremely useful and time-saving resource for regulatory information from around the world. The MedBoard team welcome feedback, and seem committed to regularly updating the system with new content and features. It’s also great value for money!” Regulatory Affairs Specialist, SME based in the UK

"Medboard has become our core resource for Regulatory Intelligence in our organisation and we hope to keep growing with them developing more tools and features that will support our team and company. We have a determination as a company to become a data driven company in terms of decision making" Business Development Manager, Large Multinational based in the USA

"The Medboard platform, one of my favourite and dynamic developed RA/QA platform for medical device industry. I still discover the real potential of this platform in my consultancy work. This platform gives me answers but at the same time generate questions. I am appreciated for real contact with developers which can remove barriers and issues immediately for each customer request. In my opinion the best RA/QA platform in 2019." Consultant 30 years experience, former Notified Body auditor

"We are extremely grateful and happy to have discovered and using this unique platform, increasing data and accessibility are two big barriers. We knew about MedBoard through TOPRA and it was a great discovery of an intelligence platform solely focused on medical devices and IVDs" Regulatory Affairs Director, Multinational based in the UK

'We have found MedBoard to be particularly useful at disseminating regulatory information throughout the company. The ease of access to the regulation, search functions and clear explanations/visuals mean that those not otherwise conversant with the regulations can easily gain clarity on any issue. For the regulatory team, it has been a particularly useful tool in planning our transition to meet the requirements of EU MDR 745/2017 and after transition we envisage it will remain a key regulatory resource for the team to ensure our continued compliance.' Regulatory Affairs Manager, SME based in UK

'When I was introduced to Medboard tool, I was not fully convinced. I thought it was just a keyword search tool. But when I started to use it, I saw all the quantity of information that comes from one search which served me on my blog. This is really the Google search for the Medical Device Regulation.'  Blog Owner and Quality Operation Manager, Large Multinational Medical Devices based in Switzerland

'A very efficient way of navigating through the new EU MDR to find the information I require, identifying the relevant annexes and highlighting the differences from the MDD' R&D Manager, SME Medical Devices in the USA

'Impressive, why this did not exist before? Incredibly impressed with its capability and particularly usability' Regulatory Affairs Director, Large Medical Devices company based in the USA.


Contact us to learn more about Customer Stories and how we provided the right solution for their needs

MedBoard is available to organizations through an annual subscription which includes any new content additions and functionality upgrades during the subscription period. We have several subscription options, suited to different company needs - register and contact our team to learn more. We will work with you to understand your business requirements so you can confidently select the right plan and solutions. 

MedBoard is composed of individuals with technical and business expertise, and many years of experience in the medical device sector. We are based in the UK, with reach and presence in Europe, and internationally. If interested or in case of any question, we are here to help, you can contact us any time.

Contact us: or through our Subscribe page


MedBoard Company - United Kingdom

6 Kerry Street
Horsforth, Leeds, LS18 4AW
United Kingdom



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