The Challenge
Regulatory professionals spend hours searching through guidance documents, standards, and updates from agencies like the FDA, EMA, and ICH. The problem isn’t lack of information—it’s too much information, scattered across lengthy documents written in complex, often ambiguous language.
Critical details can be buried in footnotes or buried within hundreds of pages. Missing a single update or misinterpreting a requirement can delay submissions, introduce compliance risks, or even block market entry. Manual search methods are slow, inconsistent, and difficult to scale across global teams.
Our Solution
Lexim AI transforms regulatory search with semantic, AI-powered intelligence. Instead of keyword matching, our platform understands the meaning behind your query and delivers precise, contextually relevant answers.
Teams can instantly find the specific clauses, requirements, or changes that matter most—whether that’s in a new FDA guidance, a revised EMA regulation, or evolving ISO standards. AI also summarizes long documents into actionable insights, making it easier to track changes and stay informed.
What Lexim AI Can Do For You
The Results
With Lexim AI, companies eliminate wasted time and reduce the risk of missing critical information. Regulatory search becomes proactive rather than reactive, ensuring your teams are always working from the most up-to-date and relevant requirements. The result: fewer delays, stronger compliance, and more confidence in decision-making.
Contact our team today to explore how Lexim AI can support your medical device compliance journey.