Online webinar

Understand the global regulatory landscape for medical devices & IVDs with Cortellis

Cortellis Regulatory Intelligence for Medical Devices and IVDs is a single, comprehensive source of global regulatory information, providing you with access to trusted content, so you can ensure efficiency and continuous regulatory compliance in the markets where you do business.

This introductory session will show you how Cortellis can answer questions such as:

  • How are products classified and what is the specific regulatory framework of medical devices, In Vitro diagnostics and combination products in a country of interest?
  • How do I compare key regulatory requirements across countries and regions and product types?
  • What are the main guidelines and regulations I need to follow and how do I keep track of changes?

The presenter will also be available to answer your questions. Join us  online to learn more about Cortellis Regulatory Intelligence in 30 minutes + optional Q&A.

  • Date:
    December 17, 2019
  • Start Time:
    9:00 am EST
  • End Time:
    9:45 am EST
  • Language:
  • Product:
    Cortellis Regulatory Intelligence