Avoid delays in product approvals and successfully bring drugs to market.
Granular information
Avoid delays in product approval and successfully bring a drug to market by building Cortellis CMC Intelligence into your everyday regulatory processes. With Cortellis, you gain access to a granular collection of CMC data requirements for drugs around the world.
"With Cortellis CMC Intelligence it’s easy for me to know which information is correct and have the reference for it."
Local regulatory requirements
Gain visibility to specific CMC requirements for clinical investigation or commercial use as stipulated by official regulations and local practices. This includes low- and middle-income countries and organizations that fund drugs and have their own set of requirements (such as the Global Fund).
“I liked the content … it was clearly laid out [and] gave information that we needed to do filings in different countries … ”
Verified data
CMC Intelligence provides access to high-quality, comprehensive and verified data for the countries where reliable, up-to-date regulatory information is hard to find. This means your CMC applications will be more accurate and completed faster and more efficiently the first time – for one country or multiple submissions.
“I think the product is really nice and easy to use … it’s good to have all the requirements in one place to be able to compare.”
Consulting services
Clarivate experts bring together a unique combination of Cortellis content and other available data sources. They provide unrivaled data science expertise, evidence-based consulting, and independent advice across the pharmaceutical R&D value chain. We have the experienced consultants and proprietary methodologies to drive life sciences innovation – faster, with independent objectivity, for better results.
