Welcome to Citeline
From early stage portfolio decisions, clinical research and development, regulatory compliance and approval, to commercial planning and analysis, Citeline offers a suite of complementary pharmaceutical business intelligence tools and solutions to support your business strategy.
When it comes to the drug development process, regulatory and compliance is one area that simply cannot be overlooked. Citeline’s regulatory intelligence, solutions, and services help ensure that your organization maintains compliance with the information, tools and services you need to achieve clinical trial disclosure, mitigate risk, increase transparency, and safeguard your brand reputation.
The industry’s leading experts on clinical trial disclosure inform our Disclose Intelligence and Management Solutions, and bespoke Disclosure Services for actionable insight you can trust.
This AI-driven enhancement automatically extracts key data elements from clinical trial protocols to populate the trial registration form and minimize manual input. The importer leverages AI to identify and map critical protocol information such as study design, arms, endpoints, and timelines — into a study sponsor's disclosure workflow to streamline the disclosure process, reduce the risk of error from manual entry, and increase compliance for confidence and control.
Contact us
Citeline Regulatory & Compliance provides sponsors with the information, tools and services they need to maintain clinical trial disclosure compliance, mitigate risk, increase transparency, and safeguard their brand reputation.
