For medical writers focused on value dossiers who streamlined, almost effortless dossier creation process

Automate the generation of complex reports and dossiers (e.g. HTA submissions) with human oversight.
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reduced draft times
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increased output
Introducing JENLY.AI
Generate and manage high-quality, evidence-backed dossiers with unprecedented speed and ease, while seamlessly integrating into your existing workflow.
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Parse and Summarize Complex Documents Instantly

Leverage AI trained for medical and regulatory content in order to extract and condense data from lengthy trial reports and dossiers—so your team drafts dossiers in half the time while skipping manual reading.

Attribute Every Statement to Its Source

Automatically link every output to source documents with clickable citations in order to make verification and compliance audits fast and painless—so quality and trust are never in doubt.

Apply Built-In HTA Templates for Country Compliance

Organize content using preloaded frameworks for AMNOG, PICO, and other HTA dossiers in order to guarantee submission-ready structure—so teams deliver compliant documents for any market without format headaches.

Automate Table and Figure Creation from Raw Data

Pull results straight into draft tables and figures in order to eliminate copy-paste errors and save effort—so dossiers include clear, accurate summaries with zero manual formatting.
Unlike generic AI tools, Jenly.ai is specifically designed for the life sciences regulatory and market access context. It “understands” HTA terminology, clinical data, and the critical importance of accuracy. This domain focus means it can handle things like complex trial endpoints or health economic terms correctly – a level of specialization others don’t have.
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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