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

 

Pharmacovigilance Webinar: Reduce Risk and Improve Compliance with Cortellis (30 min + Q&A)

 

Drug safety concerns are becoming more and more important in public health and clinical science. It’s critical to ensure that your pharmacovigilance systems are in line with regulatory obligations and are regularly monitored to increase compliance with worldwide laws, regulations, and guidelines so you can avoid delays and costly penalties.

Did you know that pharmacovigilance (PV) is one of the most consulted topics in Cortellis and that it’s the concern of 25% of the questions received by our help desk? To make it easy for you to access critical PV data, our editors have converted the existing “Pharmacovigilance and Risk Management” summaries into a consistent Question & Answer format.

Join this webinar to see how you can benefit from the new document format which addresses over 60 critical questions per country. You will also learn how Cortellis can answer questions, such as:

  • How do I search Cortellis for PV guidelines and regulations and keep track of changes?
  • How do I compare Adverse Drug Reaction reporting requirements across countries?
  • Are Safety Update Reports required for my regions?
  • How can I track drug safety issues for specific drugs?
  • Which products have Risk Management Plans in place in the US or EU?
  • What do I need to be aware of regarding device vigilance and recalls?

 

 

 

Tuesday, September 25 2018
9am San Francisco/ 12pm New York/ 5pm London/ 6pm Paris
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Wednesday, September 26 2018
9am London/ 10am Paris/ 1:30pm Mumbai/ 4pm Beijing
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Thursday, September 27 2018
9 am New York / 2 pm London/ 3pm Paris
Register

Upcoming training

 

What’s new in Cortellis (20 mins + 10 mins optional Q&A)

 

Whether you use Cortellis for competitive or clinical trials data, deals information or regulatory documents, you’ll benefit from this short “What’s new in Cortellis” webinar. In 20 minutes you’ll understand how the recent Cortellis enhancements will upgrade your Cortellis experience.

After this session, you’ll be able to:

  • Recognize drug attrition risks for companies and diseases [see below image].
  • Increase success rates for your trials by customizing timeline data (i.e. enrollment end date and endpoint completion date) to help you find the right time to run your trials and maximize patient availability.
  • Quickly and easily pinpoint regulatory medical device documents by topic [i.e. clinical trial, PV advertising] and by medical device specialty [i.e. CV, hematology, orthopedic] with brand new indexing terms.
  • Learn about similar deals so you can find the best comparable alliances and maximize the value of your asset.

We will also share some future enhancements to be released in 2018.

Join us online to learn more about these recent and future Cortellis enhancements in 20 mins + 10 mins optional Q&A:

Tuesday, 18 September
12pm New York / 5pm London
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Wednesday, 19 September
9am London / 10am Paris
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Thursday, 20 September
9am New York / 2pm London
Register

 

Upcoming training

 

Cortellis Regulatory Intelligence – 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.

 

Wednesday, September 12, 2018
9am San Francisco/ 12pm New York/ 5pm London/ 6pm Paris
Register
Tuesday, September 18 2018
9am London/ 10am Paris/ 1:30pm Mumbai/ 4pm Beijing
Register
Thursday, October 11, 2018
9am San Francisco/ 12pm New York/ 5pm London/ 6pm Paris
Register
Tuesday, October 23, 2018
9am London/ 10am Paris/ 1:30pm Mumbai/ 4pm Beijing
Register