Cortellis Regulatory Intelligence

Thomson Reuters Cortellis™, an entirely new technology platform designed to give pharmaceutical professionals like you access to the most trusted, authoritative information in a fast, intuitive way that suits you.

Whether you want to get the basics and get started fast — or fine tune your skills, Thomson Reuters can help with a variety of targeted training opportunities.

For more information about live training requests please email: CortellisLearningCenter@thomsonreuters.com

BUILD YOUR EXPERTISE ACROSS COUNTRIES WITH GLOBAL REGULATORY COMPARISONS IN CORTELLIS (45 mins)

Do you want to facilitate your regulatory planning? Discover how Global Regulatory Comparisons in Cortellis provide you with a single access point of content, regulatory expertise and visual enhancements to quickly identify common and divergent requirements across multiple countries and regions.

Save time and learn how to answer critical questions around the entire drug lifecycle, such as:

- How to prepare my dossier submission? Which countries accept online/internet submissions? Which ones do still require DVDs/CDs and paper copies?

- What are expected fees and review times of clinical trial, investigational new drug or market authorization applications?

- How to report adverse drug reactions? Which countries require risk management plans?

Join this webinar to understand which added-values this unique series of subject tables can bring to you. Connect with Rosanna Melchior, Senior Project Manager, who is looking forward to answering your questions and receiving your feedback.

Tuesday, May 6, 2014
9 am San Francisco/ 12 pm New York/ 5 pm London / 6 pm Paris
Wednesday, May 14, 2014
9:00 am London / 10:00 am Paris/ 1:30 pm Mumbai / 4:00 pm Beijing