

A breakthrough way to conduct regulatory intelligence. Stop spending time on painstaking manual work combing through multiple websites and weeding through hundreds of pages of PDFs, all while wondering if you’re identifying the comprehensive and precise content you need.
Access and interrogate FDA (CDER and CBER) and EMA regulatory documents in a single interface, and easily narrow your search based on filters and keywords.



Search and Filter
Rapidly find the precise intelligence to inform strategy and answer questions from internal stakeholders and regulatory authorities.
Identify and Summarize
Support safety surveillance by quickly identifying and summarizing adverse events mapped to MeDRA terms.
AI Chat Interface
Ask questions via AI Chat to get immediate, summarized answers based filtered source documents.Testimonials
“…a significant step forward in driving efficiencies…quickly and easily interrogate detailed health authority documents”
Vice President, Global Regulatory Affairs, clinical stage biotech company
“An impressive tool.”
Senior Vice President