Solutions
Lexim is an AI-powered regulatory intelligence tool that life science and medical technology customers use to rapidly understand, summarize, adapt, and anticipate regulatory changes. It ultimately reduces the risk of quality issues, regulatory delays, and unexpected development costs.
Industries
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Medical Device Manufacturer
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Pharma
Regulatory Agencies
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FDA
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CMS
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EMA (Europe)
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Others, by request
Solution Features
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Easily find up-to-date regulatory documents from agencies of your choice, including FDA, CMS, and others
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Review AI-generated content such as summaries, Q&As, and impact analysis to understand the content of regulatory documents faster
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Formulate questions in natural language and get high-quality answers related to any regulatory document
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Understand the connections and relevance between medical device documents and informational records from Registration, Classifications, 510K(s), PMAs to Adverse Events and Recalls
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Upload regulatory documents and apply Lexim-powered AI to generate content that increases your understanding of complex compliance-related topics
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Translate documents from 52 languages into English to improve working with medical regulatory agencies from other countries
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Use AI to generate a comparison between various regulatory documents and their versions to comprehend the relevance to your business more quickly