Expand globally with Regulatory Intelligence

Explore new markets with regulatory insights categorized by country, device type, and device class.

Chart a course – get on market – drive success

Medical device manufacturers can’t afford a one-size-fits-all approach to market expansion. To scale your success, you must navigate unique regulatory requirements in each market. RAMS is your go-to resource for defining your regulatory roadmap.

Chart a course – get on market – drive success

Medical device manufacturers can’t afford a one-size-fits-all approach to market expansion. To scale your success, you must navigate unique regulatory requirements in each market. RAMS is your go-to resource for defining your regulatory roadmap.

Get valuable insights into regulatory requirements

Understand how regulatory bodies operate in each country and how devices are classified.


Access documentation that can assist your registration.


Locate requirements and resources for in-country representation, importers, and distributors.

Make your road to market fast and worry-free

Reduce the time and cost of approval by getting it right the first time and eliminating denials.


RAMS walks you through the approvals process for medical device and IVD submissions with detailed step-by-step instructions tailored to each device class.


Get market intelligence on dossier requirements, clinical data requirements, testing, labeling, and quality management system needs.

Stay on market post-approval

RAMS Regulatory Intelligence tools include detailed post-approval guides for each market to avoid costly business interruptions.


Get the guidance you need for each market to understand: import requirements, post-approval renewals, how to address products changes, post-market surveillance, and recalls or safety concerns.

Ready for the next step? Start your free 30-day trial.

Ready for the next step? Start your free 30-day trial.