Rimsys Advanced Regulatory Intelligence

More intelligent regulatory intelligence

Easily access reliable global regulatory insights and harness it directly within automated regulatory workflows.

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Market RequirementsInsights
Keep on top of constantly changing medical device regulations to accelerate market clearance for new devices, conduct risk assessments, and respond to regulatory changes
Rimsys Advanced Intelligence
200k+ regulatory documents for over 80 countries

Access a global library of trusted medtech regulatory information that’s updated daily and translated by regulatory experts

Side-by-side country comparisons

Visually compare detailed national and regional health authority regulations with direct links to cited source documents

Detailed market entrance requirements

Use entrance requirements and historical product approval data for 50+ countries to inform regulatory strategy

Product-level linking

Associate relevant market regulations directly with product registrations, and essential principles/GSPR tables

Active monitoring

Get notified about new or changing laws, regulations, and guidance documents, and quickly assess their impact

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Use trusted regulatory intelligence across your RA processes

Product registration

Create, monitor, and manage global registrations and regulatory applications

Essential principles

Create and maintain essential principles/general safety and performance requirements (GSPR) tables

Standards management

Proactively monitor changing global standards

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