A new unique cloud platform with global data and powerful software products transforming productivity and governance for professionals, teams, and organizations.
One Platform for Clinical Research, Systematic Reviews and Evidence Management.
See MedBoard Clinical Solutions for each step of an effective Clinical Research and Compliance in a unified platform that provides ent-to-end data management.
MedBoard Search, classifications, filters, search operators, and a large number of advanced databases, tools & built in knowledge.
Time & Costs Savings
Automate, digitize and reduce extraordinary amount of work (mostly manual), with labour, repetitive tasks and processes.
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 x5
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.
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.
Ready to Get Started?
Request a free demo today to see how MedBoard can transform your research, compliance & intelligence
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, Summaries, Translations and much more.
The MedBoard platform keeps updating in real-time and growing every day!
Stay connected with what is happening
Regulatory Global Data
In more than 225 countries, access to up to date Regulatory Intelligence, data, tools and News, organized, classified and curated 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.
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 clinical research and intelligence.
Access to up to date Market Databases including Approvals, Medical Products profiles (Devices, IVDs, Drugs, Substances, Apps), Medical Manufacturers, KOLs, market news and much more.
PMS Vigilance Databases include Safety Alerts, FSCAs & Recalls, Adverse Events and Shortages. Integrated as always with advanced features and data.
Multiple software products to choose from and combine depending on your needs
Regulatory & Compliance products
SRs: Regulatory News
Review systematically Regulatory News and Updates connected to our Regulatory Global Data covering 225+ countries and 15+ regulatory areas in real time. Customize reviews, create workflows, impact assessments, actions, and reports easily with MedBoard.
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.
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 and claims, all integrated together with Regulatory Intelligence and MedBoard Search.
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.
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.
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.
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.
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.
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.
Increase productivity, collaboration, transparency and communication across your organization
Our customers report a 5x increase or more since using MedBoard
Organization-centric knowledge and collaborative platform
Seamless integration between Global Data and Software Products
Flexible approach to build processes and workflows, easy to implement
Implementing processes within your QMS or QxPs? No problem! we can also support with ready-to-use software validations, training, and work instructions.