𝗝𝗘𝗡𝗟𝗬.𝗔𝗜 is the Agentic AI Assistant for Regulatory in LifeSciences.

JENLY.AI is a specialized AI assistant for highly regulated industries such as Pharma, MedTech, and Biotech. We are transforming how regulatory, quality, and compliance teams work. Our Agentic AI Assistant drafts, updates, and manages regulatory & technical documentation, traceably, securely, and at scale. JENLY.AI enables regulatory teams to work more efficiently and productive across the product & regulatory lifecycle.

𝗪𝗵𝗮𝘁 𝗼𝘂𝗿 𝗔𝗴𝗲𝗻𝘁𝗶𝗰 𝗔𝗜 𝗔𝘀𝘀𝗶𝘀𝘁𝗮𝗻𝘁 𝗱𝗼𝗲𝘀
• Automates complex regulatory workflows: eCTDs and global dossiers; PSURs; clinical evaluation & safety reports; HTA / reimbursement dossiers. Takes both structured & unstructured inputs (PDFs, Word, Excel, past reports, literature).
• Produces traceable, auditable outputs, with statements sourced; it is GDPR-compliant, with human-in-the-loop workflows to ensure oversight.
• Built-in domain knowledge: Regulatory, Clinical, Safety, etc. aligned with regulatory requirements.

𝗪𝗵𝘆 𝗜𝘁 𝗠𝗮𝘁𝘁𝗲𝗿𝘀
Regulatory teams spend 𝘂𝗽 𝘁𝗼 𝟳𝟬% of their time on tedious and mundane tasks such as copy & paste, formatting, cross-referencing and updating. These tasks slow down approvals, increase costs, delay patient access. JENLY.AI liberates experts from paperwork so they can focus on safety, science, strategy.

Our vision: To create world where compliance runs itself – where experts are freed from administrative burden and regulatory work transforms from a being bottleneck to a competitive advantage. But JENLY.AI not only makes your regulatory teams more efficient, we help you accelerate the delivery of life-saving products!

JENLY.AI

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