Cortellis Regulatory Intelligence

Customer training and industry webinars

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.

Upcoming training

 

Cortellis Regulatory Intelligence for drugs & biologics – essentials (60 minutes)

 

Cortellis Regulatory Intelligence keeps you up to speed with the ever-changing global regulatory environment. It is a single, comprehensive source for global regulatory information that allows you to increase regulatory compliance and make faster and informed regulatory decisions.

Please join this introductory session to find out how Cortellis Regulatory Intelligence can help you answer questions such as:

  • What are the main guidelines I need to follow? How do I keep track of changes?
  • Where can I find up-to-date information on fees and easily compare them for all my countries and regions?
  • How do I market my products? What are the critical timelines I need to observe?
  • What are the regulatory requirements for pharmacovigilance and risk management?

The presenter will also be available to answer questions from the attendees.

 

Tuesday, February 12, 2019
9am London/ 10am Paris/ 2:30pm Mumbai/ 5pm Beijing
Register
Thursday, February 14, 2019
9am San Francisco/ 12pm New York/ 5pm London/ 6pm Paris
Register
Tuesday, March 05, 2019
9am London/ 10am Paris/ 2:30pm Mumbai/ 5pm Beijing
Register
Thursday, March 14, 2019
9am San Francisco/ 12pm New York/ 4pm London/ 5pm Paris
Register

 

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.

 

Thursday, February 21, 2019
9am New York/ 2pm London/ 3pm Paris
Register
Wednesday, March 27, 2019
9am London/ 10am Paris/ 2:30pm Mumbai/ 5pm Beijing
Register