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You meticulously craft regulatory submissions using Word and Excel, but face 6-12 month timelines that delay critical product launch and market entry.
Pricing
Go from Data to Submission with JENLY.AI
Automate regulatory reports. Ensure audit-ready traceability. Collaborate securely with your team.
Annual subscription, billed monthly
17% annual discount
“Jenly.ai helps us prepare dossiers in a fraction of the time. Having every statement linked to its source makes reviews much easier.”
Regulatory Affairs Manager (Pharma)
“With Jenly.ai drafting our CERs, we spend more time on real clinical work and less on formatting and copy-paste.”
Clinical Affairs Specialist (MedTech)
“Jenly.ai compiles data and drafts our PSURs automatically, so we can focus on analysis instead of repetitive tasks.”
Pharmacovigilance Scientist (Drug Safety)
“Jenly.ai keeps our HTA dossiers consistent across markets and helps us meet deadlines without the usual stress.”
Market Access Manager (Pharma / Biotech)
Explore JENLY.AI by Solution
Pharma
Pharmacovigilance
Jenly.ai auto-drafts complex safety reports, pulls and links data from any source and answers your pharmacovigilance questions on demand.
→ Read more about Solution PharmacovigilancePharma
Regulatory Submission
Jenly.ai auto-builds regulatory drafts from reports, spreadsheets, and PDFs, formats, links to sources, and gets you from chaos to first draft in minutes.
→ Read more about Solution Regulatory SubmissionMedtech
Clinical Affairs
Automate the generation of complex reports and dossiers (e.g. HTA submissions) with human oversight.
→ Read more about Solution Clinical AffairsPharma
Market Access
Automate the generation of complex reports and dossiers (e.g. HTA submissions) with human oversight.
→ Read more about Solution Market AccessDoes this sound familiar?
Your team is stretched thin, working overtime to keep up with existing submissions. As regulatory requirements expand and your pipeline grows, the manual "people + Office tools + experience" approach simply does not work any more.
Turn months of manual report writing into hours of automated drafting, with AI that ensures accuracy, consistency, and instant updates across jurisdictions.
Book a callJENLY.AI gives regulatory teams superpowers. It can read and merge information from virtually any format – Microsoft Word, PDFs, spreadsheets, databases, even outputs from literature searches – and synthesize them into a structured draft report.
Instantly Aggregate
from Any Source
Do the work of reading, merging, and synthesizing Word files, PDFs, spreadsheets, and databases in order to generate a structured, compliant first draft in minutes, so that your team spends less time on manual copy&paste and formatting and more on high-value analysis.
Auto-Cite Statements for Full Traceability
Automatically annotate every claim and data point with a clickable citation to its original source in order to guarantee audit-ready transparency, so that you eliminate errors, build trust, and streamline regulatory reviews.
Update Reports Instantly with Smart Templates
Use built-in dossier templates and real-time data syncing in order to refresh sections and formats automatically as new information arrives, so that you always meet requirements, stay consistent across jurisdictions, and never miss a deadline.
Orchestrate Complex Workflows Autonomously
Chain together multi-step tasks—like launching literature searches, retrieving new studies, and integrating findings—in order to automate the entire compliance drafting process, so that your team eliminates bottlenecks and keeps every report up to date without manual intervention.
Unlike slow, manual compliance tools, JENLY.AI slashes draft times by 75%, boosts output by over 60%, and saves tens of thousands Euro per report. We free your experts to focus on strategy, not copy and paste.
Book a callIt's time to act now!
Every year of delay in adopting AI makes the problem worse. Regulatory and compliance requirements continue to grow, so the gap between workload and capacity widens.
Inaction means accepting longer approval timelines, higher labor costs, and avoidable errors. Meanwhile, competitors who invest in AI are gaining a head-start; early adopters in pharma report tangible efficiency gains. Not moving now effectively means falling behind – in a field where speed and precision are strategic advantages.
The cost of doing nothing is paid in slower growth, higher turnover, and lost market opportunities. JENLY.AI offers a time-sensitive chance to leap forward: the sooner teams adopt it, the sooner they realize faster approvals, lower costs, and less stressed staff.
Frequently asked questions
Will our confidential regulatory data be protected?
We deploy Jenly.ai in your secure environment (cloud or on-prem), with full encryption and access controls. No sensitive data is exposed externally. We sign confidentiality agreements to reinforce this guarantee.
Can we trust the AI not to make mistakes or ‘hallucinate’?
The AI only works from your provided data and always cites the sources. To prevent it from inventing facts we implement guidelines and every sentence has a traceable origin. Crucially, experts review the draft before any submission, so human oversight catches any anomaly. Over time, trust grows as the tool repeatedly proves its reliability.
Will regulators accept AI-assisted documents?
Yes, regulators care about content quality, not the authoring tool. All Jenly.ai outputs are still vetted by human experts and formatted to official standards. In fact, explicit source citations can aid in audits and answering queries. There are no legal barriers to using AI in drafting; the end product is compliant and more transparent.
How difficult is it to integrate Jenly.ai with our current systems and processes?
Jenly.ai is designed to fit into existing workflows. It imports/exports common formats (Word/PDF), integrates via APIs to document systems, and comes with an easy UI. We provide training and support, starting with one pilot use-case to demonstrate ease-of-use. Clients report that teams pick it up quickly and appreciate the intuitive way of working.
Will this tool replace our experts or devalue our team’s expertise?
Jenly.ai acts as a co-pilot, not a replacement. In practice, users experience relief rather than fear: they spend more time on high-value work. We involve staff early, show them pilots, and emphasize that human judgment remains central. Satisfaction rates in pilot studies exceed 95% when the team sees how Jenly.ai makes their jobs easier.
Is the investment justified? What if the promised benefits don’t materialize?
We mitigate this by starting with a pilot project. You can measure real metrics (time saved, error reduction) on a trial report, before full rollout. Industry benchmarks (often 50%+ efficiency gains) strongly suggest ROI, but we also structure commercial terms to align with realized benefits. If targets aren’t met in pilot, there’s no obligation to continue. Transparent metrics and a phased approach make the financial case clear.
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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