Navigate the regulatory landscape with ease

Maintain compliance, increase approval rates and expand to new markets

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Staying current with the ever-changing regulatory landscape is challenging. If you’re not referencing the most recent guidance documents, you may be introducing unnecessary compliance risks, including citations, fines, and failed submissions – ultimately wasting time, money and resources.

We’ve removed the hard work of finding, integrating and analyzing regulatory information so you can focus on the critical decisions needed to get your products to market faster. Access Cortellis Regulatory Intelligence™ to get comprehensive, global, and expertly-analyzed information that spans all regulatory functions across the R&D lifecycle – all in one central location.

If you need a customized solution, our regulatory consultants can leverage their industry expertise and Clarivate’s robust data to fill in gaps along your entire regulatory workflow.

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Drugs and biologics

Quickly understand regulatory requirements across all aspects of therapy development.

Medical devices and IVDs

Comprehensive source of global regulatory information for medical devices and IVDs.

Mobile alerts

Get the latest updates via customized alerts sent to your smartphone with our mobile app.

Reports and analytics

Prepare for inspections, understand trends in drug approvals, discern submission requirements and instructions, and much more.

Global comparisons

Avoid the need to access multiple regulatory authority websites to understand which fit best with your strategy by quickly comparing regulations across countries.

Regulator summaries

Quickly understand regulatory requirements across all aspects of therapy development.

See how Cortellis has helped others make better informed decisions.

Don’t let regulatory complexity delay time to market.

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