Cortellis Regulatory Intelligence

Regulatory research for drug or product approvals is exactly the kind of task that eats an afternoon — searching through licensed regulatory content, cross-checking requirements across jurisdictions, tracking down the right source document. Cortellis Regulatory Intelligence connected to Neotask lets you ask a plain question about global regulatory requirements and get back a referenced answer sourced from Clarivate's Cortellis content, working within whatever regulatory documents your license covers.

• Ask natural-language questions about global regulatory requirements
• Get referenced answers sourced from licensed Cortellis regulatory content
• Navigate documents relevant to a specific drug or product approval process

What you can automate

• Cortellis Regulatory Intelligence - Ask natural-language questions about global regulatory requirements and get referenced answers sourced from Clarivate's Cortellis regulatory content. Navigate subscribed and licensed regulatory documents relevant to drug or product approval processes.

Real workflows

Check a regulatory requirement before filing

Ask Neotask what a specific market requires for an approval pathway, and it queries Cortellis's licensed regulatory content and returns a referenced answer pointing back to the source documents.

Frequently asked questions

Are the answers backed by real sources?

Yes — responses are referenced against Clarivate's Cortellis regulatory content, drawing from documents your subscription and license cover.

Does this cover every country's regulations?

It covers the regulatory content your Cortellis subscription and license give you access to, which spans global regulatory intelligence within that scope.

Plans

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