Cortellis Regulatory Intelligence

Stay informed and up to date as the global regulatory landscape continues to shift and evolve. 32% of pharma execs rated regulatory uncertainty as the highest risk in a recent survey. Cortellis Regulatory Intelligence is a single reliable source to monitor regulatory changes, understand submission routes and local practices, compare regulatory requirements across countries, and conduct pre- and post-marketing surveillance.

Cortellis Regulatory Intelligence for Medical Devices & IVDs – essentials (30 mins plus Q&A)

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 questions from the attendees.