For clinical affairs specialists at medical device and in-vitro diagnostic companies who need to gather and synthesize large amounts of information

Generate complete, compliant regulatory drafts fast—orchestrate the entire report process from data ingestion to final output with full transparency, all within one intelligent platform.
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reduced draft times
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increased output
Introducing JENLY.AI
Accelerate revenue, cut costs, reduce risk, and boost productivity—transform regulatory compliance from a costly bottleneck into a streamlined business advantage.
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Draft Complete CERs and PERs Automatically

Use an AI-powered language model tuned for medical and regulatory writing to generate coherent, structured sections—so your team produces compliance-ready drafts quickly without manual writing.

Ingest Diverse Data Sources Seamlessly

Upload Word reports, clinical PDFs, Excel vigilance data, and more using smart pipelines with OCR and domain-specific NLP—enabling accurate extraction and referencing for comprehensive drafts.

Accelerate Literature Review with AI Assistance

Automate citation screening and article summarization by interfacing with literature databases—so your team speeds up systematic reviews and focuses on critical insights.

Manage Sources with Inline Citations and Dynamic References

Attach citations directly to generated content and control references via an intuitive source panel—ensuring full transparency, easier audits, and compliant documentation.
Unlike generic AI tools, Jenly.ai is built specifically for EU MDR/IVDR with deep knowledge of CER structures, regulatory language, and MedTech terms—working effectively out-of-the-box without heavy customization.
Ready to leave manual compliance behind?
See how JENLY.AI can transform your workflow—book a call and experience faster, smarter compliance reporting today.
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