Cedience
Cedience is a Toronto-based company specializing in augmented regulatory intelligence. Their platform leverages past regulatory data, natural language processing, and machine learning to help drug development teams find evidence-backed answers to complex regulatory questions efficiently. They address industry challenges by centralizing and integrating regulatory databases, enabling quick and comprehensive regulatory research, monitoring, and collaboration. Their mission is to bridge knowledge gaps in drug development and support regulators and innovators in addressing unmet medical needs without delay.
Industries
Nr. of Employees
small (1-50)
Products
Cedience
A centralized regulatory research platform that allows querying of all product labels and review packages released by regulatory agencies at once with advanced filtering capabilities.
Cedience
A centralized regulatory research platform that allows querying of all product labels and review packages released by regulatory agencies at once with advanced filtering capabilities.
Services
Cloud-hosted platform that aggregates regulatory content and provides NLP-driven search, document comparison, extraction, monitoring, analytics, and collaboration tools for regulatory research teams.
Cloud-hosted platform that aggregates regulatory content and provides NLP-driven search, document comparison, extraction, monitoring, analytics, and collaboration tools for regulatory research teams.
Expertise Areas
- Regulatory intelligence and precedent research
- Regulatory database aggregation and normalization
- NLP and machine-learning applications for regulatory text
- Clinical trial identification and regulatory linkage
Key Technologies
- Natural language processing (NLP)
- Machine learning (ML)
- Semantic and full-text search
- Document comparison/diffing algorithms
News & Updates
An overview of the process of conducting remote regulatory assessments, including FDA guidance and evaluation methods.
Case studies illustrating FDA approvals of drugs despite not meeting primary endpoints, with detailed regulatory insights.
Cedience has analyzed over 8 million regulatory pages across 44 databases and 10 agencies.
Cedience has supported multiple case studies including REMS analysis, clinical trial support, and FDA approval insights.
An overview of the process of conducting remote regulatory assessments, including FDA guidance and evaluation methods.
Case studies illustrating FDA approvals of drugs despite not meeting primary endpoints, with detailed regulatory insights.
Cedience has analyzed over 8 million regulatory pages across 44 databases and 10 agencies.
Cedience has supported multiple case studies including REMS analysis, clinical trial support, and FDA approval insights.