Choose your path for market growth

Simple solutions that target your medical device and IVD expansion

Scalable RA/QA SaaS solution for medical device and IVD manufacturers
Select from Emergo Pro or Emergo Pro Plus for a powerful set of options to plan and grow your medical device or in vitro diagnostic device business.

Our Plans

  Emergo Pro Emergo Pro Plus
Regulatory Reports Three markets Unlimited markets
Licensed users Five users 10 users
Product Classification
Registration Tracker
Regulatory Watch
Regulatory Intelligence
Regulatory Intelligence GET STARTED GET STARTED

Sign in or sign up for a RAMS account, and for a limited time upgrade to Emergo Pro Plus for the same price as Emergo Pro.
Are you ready to leverage our regulatory expertise to navigate your path to market?


Regulatory Reports

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

  • Valuable insights into regulatory requirements
  • Understand the steps toward market approval
  • Get a guide to staying on-market post approval

Registration Tracker

Simplify your work, avoid missed renewals and save time with automated registration and certification tracking.

  • Automation saves time and avoids errors
  • Easy access to data insights
  • Instantly share information with global teammates

Regulatory Watch

Keep track of regulatory changes and how they impact you regulations

  • Get the latest news on regulatory, guidance updates
  • Find updates affecting your device
  • Structure your updates to plan your work

Regulatory Intelligence

Plan your expansion with process charts and FAQs that comprise a global knowledge base

  • Visualize regulatory pathways and timelines
  • Answer questions about new markets
  • Strategize for success post market approval

Product Classification

Keep track of regulatory changes and how they impact your registration

  • Intuitive process saves time, eliminates uncertainty
  • Verify an existing classification and ensure you're on the right path
  • Start your road map to market with confidence


Rams includes regulatory process charts on new markets, which weren't available before, that medical device companies might want to explore. Consolidating them all into one location makes it easier for customers worldwide.

Yes, it's free to register for RAMS. Some premium services, such as Registration Tracker, Regulatory Updates, and Regulatory Intelligence available for a free 30-day trial. Log in for details.

Yes. If your 30-day free trial has expired, you will need to renew your account.

Yes, you can add as many teammates to your RAMS account as you wish. You can also control their access to view and modify registrations. You can even create accounts for your distributors and allow them to only view registrations for the products they distribute.

Ready for the next step? Register today.

Ready for the next step? Register today.