More intelligent regulatory intelligence
Easily access reliable global regulatory insights and harness it directly within automated regulatory workflows.
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Access a global library of trusted medtech regulatory information that’s updated daily and translated by regulatory experts
Visually compare detailed national and regional health authority regulations with direct links to cited source documents
Use entrance requirements and historical product approval data for 50+ countries to inform regulatory strategy
Associate relevant market regulations directly with product registrations, and essential principles/GSPR tables
Get notified about new or changing laws, regulations, and guidance documents, and quickly assess their impact
Use trusted regulatory intelligence across your RA processes
Create, monitor, and manage global registrations and regulatory applications
Create and maintain essential principles/general safety and performance requirements (GSPR) tables
