One Platform, Endless Knowledge and Solutions

for MedTech | Pharma | Life Sciences

A new unique cloud platform with global data and powerful software products transforming productivity and governance for organizations, teams and professionals.

Your Research, Intelligence, Compliance, Work and Data Management on one unified platform

Regulatory | Clinical | Market | PMS 

We’re here to simplify and unify your transformation.
One big data platform, and multiple software products for all your needs.

100+ Customers rely on us

Trusted by many leading and innovative organizations. From Start-Ups to Large Companies.

Security and Trust

Your security and privacy is our priority.
ISO/IEC 27001 is widely known for providing requirements of an Information Security Management System (ISMS).
It is the gold standard for policy and management controls around information security. MedBoard is ISO 27001:2022 certified.
 
 
 

MedBoard Platform:

Global Data + Software Products

 

G

Global Data

MedBoard Search, News & Databases

MedBoard Global Data and Intelligence Platform is huge, we mean, it is actually very huge! (over 1 Billion connected datapoints), providing global access to up to date information, data and knowledge.

MedBoard only uses trusted sources, and provides continuous and instant access in real-time to information and data, covering News, Databases, Intelligence, Profiles, Analytics, Tools, Documents, Webpages, Curated Summaries, Translations and many more resources at your fingertips any time.

The platform keeps updating in real-time and therefore growing every day! Keep yourself informed, be fast, be the first, and stay connected with what is happening.

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Regulatory

Access to up to date Regulatory Intelligence, data, tools and News in more than 225 Countries, organized, curated and cleaned by MedBoard.

With a coverage of 15+ regulatory areas, including MedTech, Pharma/BioTech and Clinical trials, that includes countries curated summaries for an unparallel research and intelligence.

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Clinical

Access to up to date Clinical databases and information, including Clinical Trials & Studies, Literature, Guidelines, Hospitals and Clinics, professionals & KOLs, medical conditions and treatments, clinical news and much more.

Integrated with advanced filters, analytics and integrations with other MedBoard databases, for a faster research and intelligence.

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Market & PMS

Access to up to date Market Databases including Approvals & Registrations, Medical Products profiles (Devices, IVDs, Drugs, Substances, Apps), Medical Manufacturers, Professionals and KOLs, market news and much more.

PMS Vigilance Databases include Safety Alerts & Communications, FSCAs & Recalls, Adverse Events and Shortages. Integrated with advanced filters, analytics and integrations with other MedBoard databases.

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“MedBoard is impressive, nothing compares to it”

Software Products

SRs: Regulatory News

Review systematically Regulatory News and Updates connected to our Global Data covering 225+ countries and 15+ regulatory areas in real time. Customize it, create protocols, impact assessments, actions, and reports easily with MedBoard.

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SRs: Literature & Clinical

Review systematically Literature and accelerate your systematic review workflow from search to reporting. Whether you import automatically results or import results from your own databases, MedBoard software and AI-features will simplify and customize to your needs the process, search, review and reporting.

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SRs: Market & PMS

PMS Adverse Events, Recalls, FSCAs, Safety Alerts, Approvals and Registrations, press releases, media news, and many more databases where to choose to perform Market, Post-Market Surveillance (PMS) and Vigilance monitoring.

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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 teams and professionals. 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. 

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Compliance Manager

Organize, manage and track your compliance evidence with the Compliance Manager. This module helps to identify and control the specific regulations, guidance, standards, procedures, technical documentation that apply to you, and to organize, action, and track your related compliance evidence

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Reference Manager

A reference management software to manage your references, bibliography and PDFs. Including features such as duplicates and custom tags, and seamlessly integrated with your MedBoard Literature Systematic Reviews, MedBoard products and data, to keep all your clinical evidence connected in one place.

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Market Lists

Create custom lists with Manufacturers, Products, Substances, Hospitals, Researchers, KOLs, and manny more types 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. 

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Products Information

A powerful ready-to-use Products Information Management to organize, manage and track information about your products, product codes, SKUs, and its information, including Unique Identifiers (e.g. UDI), all integrated together with Regulatory Intelligence and MedBoard Search. 

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Country Registrations RIMS

A powerful ready-to-use Country Registrations RIMS to organize, manage, and track information about your countries registrations, certificates, licenses and economic operators, all integrated together with Regulatory Intelligence, Regulatory Reviews, Task Manager and MedBoard Search.

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Increase productivity, collaboration, transparency and communication across your organization

Organization-centric knowledge and collaborative platform

Many Testimonials & Customers Success 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!! "
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 EU 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 with this platform! MedBoard has transformed the productivity of the whole department in no time. And it keeps evolving rapidly! "
VP Regulatory Affairs
" 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. "
Senior Research Officer
" Being on top of the latest vigilance information for our products and competitors gives us a huge advantage for patient safety, risk identification, SOTA, and competition monitoring and trends. What used to take me weeks now takes me seconds, and personalised to our needs. "
PMS & Vigilance Director

Seamless integration between global data and software products

Flexible approach to build processes and workflows, easy to implement

Processes within your QMS or QxPs? No problem! we can also support with ready-to-use software validations, training, and work instructions.

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 demand 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, one-solution, and most, still, very 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.

Why Organizations choose MedBoard

MedBoard unique approach provides instant benefits:

 

Information Access

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

Time & Costs Savings

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

Easy to Use

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

Productivity Increase

Our platform allows teams to fully customize their experience and increase their efficiency massively in processes and access to information.

Multiple Solutions

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

Customization & Trust

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

MedBoard let you focus on what truly MATTERS

How many medical industry 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. This is even getting worse and worse over the last years.

And most important: 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.

Recognized by the leaders and experts. Loved by customers

Information and data that you can trust. Built by 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.

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We make information accessible,
and processes more efficient

while keeping control and compliance,
in one connected place.

 

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