Regulatory Intelligence (RI)

For MedTech, Digital Health, and Pharma

In Regulatory Intelligence (RI), it is equally important the information collected and reviewed through EXTERNAL sources as the information collected internally through your INTERNAL sources and experiences. Both streams will provide you a very comprehensive RI programme. MedBoard offers tools and services for you to build this for your organization.

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 MedBoard Regulatory Intelligence Toolkit:


Regulatory News from 225+ Countries
Systematic Review & Assessment of Regulatory and Standards News tools
Affected Products Assessment linked to Organization Portfolio
225+ Countries Profiles
50k+ Documents, Guidance, Regulations, and Consultations
30k+ Technical Standards Profiles and updates
100,000+ Countries Regulatory Summaries
Countries Regulatory Flowcharts for Market Entry and Modifications
20k+ Regulatory Requirements Summaries
Translations: Document & News
Regulatory Databases: Approvals, 510(k)s predicates, Warning letters, Inspections, etc.
Trackers for Regulations
Technical Standards Databases: adopted
GAP summaries
and much more

 Ask Regulatory Questions & Requirements to MedBoard Search and get quick answers for 225+ Countries:


Keep on top in a Systematic and Structured way

RI is essential for organizations in order to continuously evaluate, monitor requirements and impact for their Products, Organization, QMS, Registrations, Clinical trials, Manufacturing, etc. that may affect the organization, but also to anticipate events or have a safety net and better preparation.

Regulatory Intelligence is mainly responsible, but not limited to, for:

  • Monitor regulatory updates and trends for impact assessments
  • Identify opportunities, pitfalls and risks, from product compliance to revenue losses or impact
  • Registration status impact and new requirements approach
  • Prioritization and input to your organization strategy and actionable steps

The solutions provided in the MedBoard platform will allow you to be on the top of the game.

Better and More Robust Compliance with less effort

Automated workflows and structures reviews, combined with up to date resources eliminate cumbersome and manual, repeated and tedious tasks. In addition, it minimizes human errors.

Process gets implemented as per organization or team, regardless individual use, allowing to have much better consistency and robustness, creating a single repository and organization-centric knowledge.

The most complete suite of Regulatory Resources 

Medboard approaches Intelligence from many angles and that is why we built many different resources, providing an unparallel combination and offer to the regulatory professionals.

And all of this, built on top of MedBoard Search.

An extensive wealth of Regulatory news, information, data and tools

Customer Stories

VISION RT  Medical Devices Manufacturer

 MedBoard has streamlined our Regulatory Intel and PMS activities, removing the need to spend hours every month trawling regulator websites for information. The platform is user friendly and the MedBoard team is incredibly responsive. “

GUERBET –  Pharmaceutical Manufacturer

 I have found its Regulatory Systematic Reviews process to be easily incorporated into our existing procedures. It is also very helpful for Regulatory preparation for Management Reviews

ENDOMAG – Medical Devices Manufacturer

 MedBoard’s databases and regulatory tools make collating news, research, and intelligence easy to manage for a regulatory professional. This platform is intuitive and easy to navigate, and has been invaluable for staying up to date on all regulatory activities worldwide

An Easy to Use, Powerful and Accessible Platform for Organizations of every size

Ready to Get Started?

Request a free demo today to see how MedBoard can transform your evidence transformation journey