01
Medical information
Help specialists retrieve and explain approved information while preserving source and review requirements.
Industry
Pharmaceutical
Medical AI assistance for evidence-heavy workflows, medical information, patient education, and responsible human escalation.
What Lunas supports
- Evidence-aware medical information support
- Readable, approved patient and professional education
- Clear boundaries for safety, regulatory, and clinical review
The opportunity
Why this work needs medical context
Pharmaceutical work combines large evidence sets with strict requirements for accuracy, version control, approved claims, safety reporting, and professional accountability. A fluent answer is not enough; the source, boundary, and reviewer matter.
Lunas is suited to the preparatory layer of that work. Today a specialist can use Stethos to understand and organize permitted material, while a future Team & Enterprise workspace and governed Stethos API can govern who can use which content, how responses are reviewed, and where regulated issues are escalated.
Where Lunas fits
Useful work before the final decision
Stethos helps explain, organize, and investigate. People and qualified professionals stay responsible for the decisions that follow.
02
Evidence review
Structure literature, study reports, and open questions for qualified scientific review.
03
Patient education
Make approved information easier to understand without personal prescribing or promotional overreach.
04
Safety handoff
Identify conversations that belong in established adverse-event and product-quality processes.
A practical workflow
From a question to human review
A repeatable path makes the model easier to supervise and the result easier to trust.
- 01
Govern the source set
Define approved, current material and who is allowed to use it.
- 02
Assist the work
Use Stethos to summarize, compare, draft, or explain within the defined boundary.
- 03
Route regulated issues
Send clinical, safety, quality, and promotional questions to the designated function.
- 04
Review and record
Require accountable approval and retain the context needed for quality oversight.
Product path
Start with Lunas today. Grow into governed workflows.
Lunas.One is available to individuals today. Team & Enterprise workspaces and a governed Stethos API are in active development — the roadmap below is directional, not a promise of present availability, and larger deployments will require the right privacy, security, evaluation, and human-review controls.
Available in Lunas
- Medical file and evidence conversations in Lunas
- Lab workspaces for structured investigation
- Safety-oriented prompt and access foundations
Team, Enterprise & API direction
- Team & Enterprise governance and approved knowledge spaces
- Review queues, roles, and organization audit controls
- A governed Stethos API for validated pharmaceutical workflows
Questions
What people usually want to know
Can Lunas provide prescribing advice?
No. Prescribing requires a qualified professional with the complete patient context and applicable product information.
Can it automate adverse-event reporting?
Lunas may eventually assist with intake and organization, but regulated reporting requires validated processes, defined responsibilities, and human oversight.
Can teams restrict Stethos to approved content?
That is a core requirement for future enterprise deployments. The current individual product is not presented as a validated pharmaceutical knowledge or regulatory system.
Try the product
Bring one real health question into context.
Use Lunas for information and organization, then involve a qualified professional whenever a health decision is needed.