Accelerate Pharmaceutical Compliance with RegIntel for Pharma
Built on the Lexim Praxis platform, RegIntel for Pharma helps pharmaceutical companies move faster—without compromising compliance. With AI at its core, it simplifies regulatory workflows, aggregates global requirements, and delivers insights that support better, faster decision-making.
RegIntel’s Business Impact
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80+ Global Agencies | 5,000+ Guidance Documents with Analyses | 1,600+ Standards Information | 100M+ Device Data Points |
RegIntel™ for Pharmaceuticals
What You Can Do with RegIntel for Pharma:
Global Regulatory Intelligence: Access up-to-date pharmaceutical regulations, guidelines, and directives from 80+ countries, including the USA and EU.
Agent-Powered Automation: Automate routine tasks like submissions, document comparisons, and data extraction using pre-trained AI Agents. Your team focuses on strategy, not paperwork.
Smart Document Chat: Converse directly with your regulatory documents to ask questions, get precise answers, and unlock document insights instantly
Predictive Compliance Planning: Use AI to foresee regulatory hurdles and adjust your development plans early—avoiding costly delays.
Real-Time Data Insights: Tap into 100M+ data points covering drug approvals, clinical trials, adverse events, and more. Make informed, data-driven decisions.
What Our Clients Say
Tatyana G., Vice-president of Regulatory Affairs
"Lexim helped my medical-device company gain a deep understanding of AI and its applications to Regulatory Affairs."