Technology & It Solutions

The Regulatory, Research & Intelligence Platform

for MedTech | Digital Health | Pharma

Whether you are a small organization or a large enterprise, our MedBoard Platform connects news, information, data, individuals, teams & processes, so you can put action, intelligence, evidence & compliance at the centre.

Trusted by many Leading and Innovative Organizations, discover a new exceptional access to information and digital solutions

Platform Content Access and AI Powered Research

MedBoard Search

Search the world’s MedTech, Pharma & Digital information with MedBoard, it delivers up to date Regulatory, Clinical, Standards, Clinical, Market and PMS information in more than 225 Countries. 

Our Information Portal & Individual databases are curated with only trusted sources and covers more than 1 Billion data points. News, Databases, MedBoard Profiles, Webpages, Documents, Content, Media and much more in just one click.

Advanced Filters, AI Evidence Classification and Categorization. Powerful, Up to Date and Continuously Organized.

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MedBoard Platform Content Access

MedBoard is huge, and our Menu provides access to dedicated Regulatory, Clinical, Market, PMS, Standards areas in 225+ Countries, with:

News: Real-Time News from millions of sources such as Authorities, Manufacturers, Clinical Sources, Experts, Hospitals, and any trusted relevant medical stakeholder or source.

Databases & Analytics: 50+ Individual Real-time Trusted Regulatory, PMS, Clinical & Market Databases, with Analytics & Insights. Databases include Clinical Trials, Recalls, Literature, Adverse Events, Regulatory News, Products updates, and many more.

MedBoard Profiles: 10+ Millions of Profiles with integrated data and updates: Countries, Products, Manufacturers, Hospitals, Standards, KOLs, Medical Conditions, Medical Terms, Regulatory Requirements, and many more types.

Intelligence: Databases, Insights & Content, plus curated human intelligence such as 100k+ Country Regulatory Summaries in 10+ Regulated Areas.

Resources & Tools: Tools, Document Viewers, Translations, Periodic reports, flowcharts, 510(k) Tree Navigator, Dictionaries, Trackers, etc.  

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Professionals get impressed after the first demo, are you ready too to experience something new?

Enterprise Professional Solutions

Systematic Reviews

Our unique Systematic Review solution is integrated with 100+ large MedBoard databases and thousands of sources, providing seamless integration with trusted data, and embedded with easy to use and state of the art tools.

Our customers can select from 25+ Types of Systematic Reviews, for Clinical Literature, but as well for Regulatory News, PMS Recalls, PMS Adverse Events, Technical Standards, Market Information, Clinical Trials and many more, taking the organization to the next level in consistency, automation and evidence quality! 

Smart features include: Automated Processes, Appraisal tools, Data Extraction, Reviewer Assistant, Customization features, PRISMA Flowcharts, and SRs grouping for projects and plans.

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Lists Monitoring

Create custom lists with profiles from the 10M+ MedBoard Profiles vast collection to analyse changes in statistics/analytics by custom date periods, add intelligence, tags, notes, reviews, and much more in only one place.

Aggregate in each list the profiles that you need for the project or goal. We have lists for Manufacturers, Products, Authorities, Standards, Healthcare Providers and soon KOLs. This is widely used for Research, Intelligence, Due Diligence and Clinical Evaluation Reports.
Key and essential to understand changes and trends from manufacturers and products, the evolving landscape, SOTA, due diligence and many more uses. 

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Product Portfolio Management

A powerful Off-The-Shelf and Ready-to-use Portfolio Management to organize, manage and track information about your products and its information, including UDI, all integrated together with Regulatory Intelligence and MedBoard Search.

This module integrates also with other modules such as Country Registrations, and have extensive data features and functions.

Ideal for Manufacturers, Authorised Representatives, Providers, Distributors and other Operators in the MedTech industry.

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Country Registrations RIM

A powerful Off-the-Shelf and Ready-to-use Country Registrations RIM to organize, manage, and track information about your countries registrations, certificates and operators, all integrated together with Regulatory Intelligence and MedBoard Search.

This Regulatory Information Management includes as well a Renewal Management and this module integrates also with other modules such as Product Portfolio, Regulatory Systematic Reviews and Task Manager, to keep on top and perform change evaluations and assessments.

Ideal for Manufacturers, Authorised Representatives, Providers, Distributors and other Operators in the MedTech industry.

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Task Manager

The Task Manager integrates with MedBoard data and modules to easily action, track, and complete efficiently any task and project by organization, team and person.

Customize your workflow, and view your projects as a Task List or Board View. Easy to use, with intuitive UI to help you get started fast. Scale ready with other modules when it is time to grow. 

Imagine being able to action the 1 Billion+ datapoints plus your Reviews, Portfolio, Registrations, Operators, Changes, Competition, and more in MedBoard, the Task Manager makes it possible, and bring collaboration and transparency to your organization.

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Premium Intelligence

On top of the Regulatory Intelligence, Clinical Intelligence & Market Intelligence delivered across the whole platform, MedBoard also creates and provides synthetic and human intelligence in the form of summaries and flowcharts that we keep up to date daily.

We keep up to date 100,000+ Regulatory and Clinical Summaries, curated by experts and continuously evolving and updated as new changes take place. In Premium Regulatory Intelligence, we offer regulatory requirements summaries for more than 225 Countries in more than 10 Regulated Areas!

A very essential activity for any medical organization in this very fast changing landscape. 

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Compliance Portfolio

Organize, manage and track your compliance evidence with ready-to-use and up to date global templates for assessments, checklists and more.

Ready to use templates for 225+ Countries related to Regulations, Guidance, Essential Principles, MDSAP, Audit preparations, Declarations, and much more. Export when you need it in our preferred formats.

Stay compliant and on top, keep in existing or go to new countries, explore new requirements faster, with ready to use templates and AI support, embedded with the latest news of MedBoard Search and MedBoard Intelligence.

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Testimonials & Customers Stories 


MedBoard is simply amazing and saves me valuable time and effort conducting research and staying up-to-date on changes around the globe. Absolutely the best value for medical device data !!! 

Regulatory Affairs Director  

“Having access to a digital platform that acts as a single repository for Regulatory Intelligence, Market Intelligence and Clinical Evidence allows us to automate the laborious tasks and focus on the more technically demanding process. MedBoard is simply, practical tool that offers real value to the organization.”

VP Clinical Affairs & Marketing

It is our main source for MDR compliant scientific literature searches and post market surveillance. It has been instrumental to optimising these processes by centralised, automated searches, precision of keyword sub-searches, traceable screening and appraisal and useful export functions. We would highly recommended to the medical device industry! 

Clinical Evaluator & Project Manager

” WOW!! I am just impressed 

Regulatory Affairs Director

” We are enjoying using MedBoard very much. The combination of scientific, regulatory and market information in one well organised place is very appealing to us. It has significantly reduced the amount of time and effort we spend in many areas. It has been especially helpful for our various regulatory document needs, including following specific regulatory bodies and getting update notifications on regulations. The Literature Search monitoring and traceability has been very useful, and the recent upgrades will make our future use significantly easier.”

Senior Research Officer

Increase collaboration and communication across your organization

A Multi-Use platform with endless applications: 


Why MedBoard?

The Growing and Long-Term problem that MedBoard Solves

1. An extraordinary increase in flow and speed of news, articles, information and data shared from key sources (e.g. authorities, clinical, manufacturers) that require planning, collecting and reviewing. In addition, there is a growing challenge of ensuring trusted sources and information.


2. A significant increase in de
mand and organization for
 data, information, and evidence from key stakeholders (e.g. authorities, payers) and internal processes, and new and increasing larger and more complex requirements for Documentation, Reports, PMS, Clinical Literature review, and data analysis.


  Existing solutions are expensive, tedious, cumbersome, and most, still, manual

To start with, none has this amount of data organized, searchable and up to date as MedBoard. Other solutions or alternatives are either manual processes, expensive outsourcing, or repeated searches with no consistency through multiple sites and databases, looking into unstructured and unorganized datasets and manually importing the data.

The MedBoard Approach

The most powerful all-in-one platform while decreasing costs dramatically


Why Organizations choose MedBoard

MedBoard unique solution is built with the most advanced research features and techniques and integrated into databases and thousands of sources (including importing options), providing seamless integration with trusted data, and easy to use and state of the art tools.


Powerful Search &
Information Access

MedBoard Search, classifications, filters, search operators, and a large number of advanced databases, tools & built in knowledge

Time & Costs Big Savings

Reduce extraordinary amount of work (mostly manual), labour, repetitive tasks and processes with automation, digitization and customization.

Easy to Use & Friendly UI

Customers report 'Easy to Use' and friendly UI as one of the top reasons to use MedBoard, we are transforming complex processes into easy steps.

Multiple Enterprise Solutions

MedBoard is a multi-use platform, providing many solutions in just one place, in addition to incredible access to information and data.

Enterprise Ready

Security, Compliance and Privacy built in features, including SSO are available to our customers. Our platform is also easy to scale for larger customers.

Customization & Teams

Our platform allows teams to fully customize their experience (e.g. review process) and to connect with colleagues and previous work.

Changing Professionals Lives & EMPOWERING them

How many medical professionals with many years of experience, degrees, masters, Phds, are manually searching and doing repetitive tasks, when performing reviews or reporting, or even checking the latest updates. This is mostly due to manual and tedious work (searches, monitoring, reviews and reporting). This is even getting worse and worse over the last years with the unprecedented increase of amount of data shared by Key stakeholders. 

And Most Important Question: How are these affecting the quality of life of these professionals? “why high-level professionals should spend hours and hours searching in many locations, or copying and pasting, or other tedious task, instead of applying their knowledge and experience?”  We want to change this.

More Accessible & Affordable medical industry information and data, for ALL


We think of the big picture, more accessible information for ALL stakeholders will increase patient safety, innovation, faster execution and quality of life of professionals and patients. 

We think of MedBoard as a MUST TO HAVE for any organization working in the life sciences sector. Every organization, regardless their size, should access to and afford such a resource. Pricing to accessible quality databases that are critical for patient safety and medical professionals should never be a barrier. MedBoard is also cloud based and ready-to-use solution. 

TRUSTED by leading and world’s best life science organizations of every size. Thousands of users.


Information and data that you can trust. Built by Medical Professionals that already been working in the industry for many years, and Powered by Data Science, engineering and AI. We understand the industry, we understand your challenges and we have great passion for innovation.

A large number of Manufacturers (Medical Devices, In Vitro Diagnostics, Biotech, Pharmaceuticals), Consulting Companies, Providers, Research Organizations and even Governments and Agencies trust and already use MedBoard. The profile of our customers are agile, think-forward, proactive organizations with great understanding of the challenges and the need for adoption of digital solutions.

Trusted, Used and Evaluated by top experts in the industry

Our software has been evaluated by a great number of experts in the industry, which continue to collaborate or work with us. In addition, more formal external evaluations have been taking place and for example, we are proud to have obtained a Digilab Certificate “Certificate for Regulatory Software” issued by the German Company Metecon .

Ready to Get Started?

Request a free demo today to see how MedBoard can transform your evidence, compliance & intelligence transformation journey