Cedience

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Teams are spending hours searching through different databases to answer questions on regulatory expectations, past approvals and precedents.

Cedience is an AI-powered regulatory intelligence platform that answers your most complex questions almost instantly while helping you monitor the changes in the regulatory environment and the competitive landscape.

Here are just a few examples of the questions Cedience helps you answer.

Schedule your demo here and come meet our team at booth 1740

- What are FDA's guidelines on immunogenicity testing?

- Which products are approved for ulcerative colitis?

- Which endpoints have supported past approvals in triple negative breast cancer?

- Are there examples of FDA approval despite a failed primary endpoint?

- Which products are approved for Diffuse Large B-Cell Lymphoma (DLBCL) and have a warning for hepatotoxicity?

- Which products or companies have been granted Rare Pediatric Disease Designation (RPDD) and for which conditions?

Products and Services
Artificial IntelligenceClinical R&DClinical Trial DesignLabeling ServicesPreclinical Development and Early-Phase Clinical ResearchRegulatory Affairs/Regulatory StrategyRegulatory CMC and Product QualityRegulatory IntelligenceRegulatory Policy
Date(s) & Times of Booth Activities
All Days & Times
Description of Booth Activities
Join us at the booth for a live demo of our AI system and see how it can answer your intelligence questions almost instantly.
Booth Giveaways
4 x $100 Amazon Gift Cards

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