Easily find up-to-date regulatory documents from agencies of your choice, including FDA, CMS, and others
 

Review AI-generated content such as summaries, Q&As, and impact analysis to understand the content of regulatory documents faster  
 

Formulate questions in natural language and get high-quality answers related to any regulatory document
 

Understand the connections and relevance between medical device documents and informational records from Registration, Classifications, 510K(s), PMAs to Adverse Events and Recalls
 

Upload regulatory documents and apply Lexim-powered AI to generate content that increases your understanding of complex compliance-related topics
 

Translate documents from 52 languages into English to improve working with medical regulatory agencies from other countries
 

Use AI to generate a comparison between various regulatory documents and their versions to comprehend the relevance to your business more quickly