A Liorta platform
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An AI-powered SaaS platform for Life Sciences.
Lorgani is Liorta’s AI-powered SaaS platform for Life Sciences, designed to transform complex structured and unstructured information into organized, traceable and decision-ready outcomes for regulated environments.
- Evidence-connected outputs
- Traceable to source
- Expert review built in
- Protection by design
- Purpose-built for regulated Life Sciences
Explore the capabilities
These capabilities work together as a whole - not as a fixed sequence of steps.
Liorta company Lorgani platform iDossi · CliDossi · ConDatics applications
More than dossiers
One foundation for the information-intensive work of Life Sciences.
Regulatory dossiers are where Lorgani is focused first. The same foundation applies wherever complex structured and unstructured information has to become organized, traceable and decision-ready - across safety, clinical, scientific, quality and analytical work.
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Kinds of input
- Documents
- Literature
- Tables
- Reports
- Structured data
- Unstructured information
- Data & system sources
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Kinds of outcome
- Structured dossier
- Clinical report
- Structured data
- Analytics
- Decision-ready report
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Applications
Designed for regulated work
What stays true in every application.
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Evidence first
Outcomes are grounded in the source material behind them, and remain traceable to it.
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Protection by design
The Liorta Protection Engine is designed into AI-assisted work to help safeguard designated sensitive and confidential information.
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People decide
Review, judgement and approval stay with qualified professionals. The platform prepares; people decide.
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Governed progression
Work moves through review, revision and approval in a controlled, recorded way.
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Built for Life Sciences content
Designed around the documents, evidence and conventions of regulated Life Sciences - not adapted from generic tooling.
Why Lorgani
Quality first. Efficiency second. Control throughout.
The order matters. In regulated work, speed is only valuable when the output can be trusted - so quality comes first, efficiency follows, and your teams stay in control of every decision that matters.
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Quality first
Outputs are structured to the document standard, connected to their evidence and reviewed by experts before anything is finalised. If it cannot be trusted, it is not finished.
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Efficiency second
Once quality is secured, the searching, assembling and reformatting that consume expert time fall away - so work moves faster without cutting corners.
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Control throughout
Your teams decide what is prepared, reviewed, revised and approved. Work moves forward in a governed, recorded way, and nothing is final without human approval.
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Auditability built in, traceability in one click
Drafts, revisions and decisions are recorded as the work happens, and any statement can be traced back to its source in a single click - ready for review, audit and inspection.
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Blinded AI™ - protection from the AI, not just around it
Many platforms protect sensitive data around the AI. Lorgani protects it from the AI: designed from day one so that AI works blind to designated sensitive and confidential data, through the Liorta Protection Engine, so intelligence can be applied without exposure.
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Ready in 15 minutes*, built to scale
Your organization and tenant configured and ready to start in 15 minutes*, on an enterprise SaaS platform built to perform reliably and to grow with your products, teams and markets.
* Terms & Conditions apply. Configuration of the organization and tenant in 15 minutes applies when starting with Liorta's standard templates and workflows for one product, or with the product data file (JSON) ready and a single user.
Lorgani vs general-purpose AI
Built for regulated Life Sciences work - not adapted to it.
General-purpose AI is powerful, and manual assembly is familiar. Regulated documents need both intelligence and accountability, applied to the right evidence.
| Aspect | Lorgani | General-purpose AI assistants | Manual assembly |
|---|---|---|---|
| Built for | The documents, evidence and conventions of regulated Life Sciences - from DSURs and PBRERs to clinical and quality documentation | Any topic, for any user | Whatever each team has built up over time |
| Link to evidence | Content stays connected to the source evidence behind it | Varies; answers are not tied to your controlled evidence set | Maintained by hand, reviewer by reviewer |
| Human accountability | Expert review and approval embedded at critical points | Left to the individual user | Yes - but expert time goes on assembly rather than assessment |
| Sensitive information | Protection designed into AI-assisted work (Liorta Protection Engine) | Depends on the tool and how it is used | Depends on local practice |
| Consistency | Supports consistency with prior reports and related documents | Each answer starts from scratch | Hard to maintain across cycles, teams and markets |
| Governance | Review, revision and approval move forward in a controlled, recorded way | Outside the tool | Tracked in separate systems and email |
Lorgani Applications
Purpose-built applications. One intelligent foundation.
Different applications. Different outcomes. One Lorgani platform.
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™Transform heterogeneous source evidence into structured, traceable and reviewer-ready aggregate safety reports and regulatory dossiers.
Explore iDossi -
™Apply Lorgani to complex clinical and evidence-intensive documentation and reporting.
Explore CliDossi -
™Transform information across documents, content and structured sources into structured data, analytics, reports and decision-ready outputs.
Explore ConDatics
Questions
Frequently asked questions about Lorgani
What is Lorgani?
Lorgani is Liorta’s AI-powered SaaS platform for Life Sciences, designed to transform complex structured and unstructured information into organized, traceable and decision-ready outcomes for regulated environments.
What kind of work is Lorgani designed for?
Information-intensive work in regulated Life Sciences: regulatory and safety dossiers, clinical and medical documentation, literature and evidence, quality and compliance, and content-to-data analytics. Regulatory and safety dossiers are where Lorgani is focused first.
Which applications run on Lorgani?
Purpose-built applications share the same Lorgani foundation: iDossi for aggregate safety reports such as the DSUR, PBRER/PSUR and PADER; CliDossi for clinical documentation; ConDatics for turning content into structured data, analytics and decision-ready reports.
How does Lorgani keep its outputs trustworthy?
Lorgani is designed to produce high-quality, evidence-connected outputs. Content stays traceable to the source material behind it, and expert review is embedded at critical points to strengthen confidence, traceability and governance.
Does AI make the final decisions?
No. AI brings speed and scale to preparing and organizing information; review, judgement and approval stay with qualified professionals. The platform prepares - people decide.
How is sensitive and confidential information protected?
The Liorta Protection Engine is designed into AI-assisted work to help safeguard designated sensitive and confidential information, with governed processing, traceability and human oversight. Detailed security information is shared with prospective customers through a structured, confidential review with Liorta.
Is Lorgani suitable for regulated environments?
Yes - Lorgani is designed for regulated Life Sciences environments. Liorta's security and trust approach is grounded in verifiable controls, transparent governance and recognized standards, with certifications and regulatory references used where independently validated.
How can we get started with Lorgani?
Talk to Liorta about the work you want to improve - for example a specific aggregate report or document type. We will show what is relevant to you in a focused demonstration.