01
Work the literature
Compare uploaded study reports and papers in one project.
Industry
Pharmaceutical
What individual pharma professionals can use today — evidence reading, terminology, patient-education drafting — with governed team tooling on the roadmap.
What Lunas supports
- Lab projects for literature and study-report work
- Plain-language drafts of complex approved material
- Comparison across uploaded evidence sources
The opportunity
Why this work needs medical context
A medical-information specialist gets asked about an interaction buried across three study reports and a label. The evidence exists; assembling and explaining it under time pressure is the work.
With an individual Lunas account, that specialist can load the documents into a Lab project and work through them with Stethos: what each source says, where they differ, how to phrase the answer plainly — then run the result through the medical-review process the company already requires. The same applies to a writer turning approved material into readable patient education.
What pharma organizations ultimately need — approved-content boundaries, review queues, audit — is roadmap territory; today Lunas sharpens the individual professional.
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
Explain plainly
Draft readable versions of approved material for proper review.
03
Track the reasoning
Keep sources, notes, and conclusions attached to each question.
04
Hand off safety
Recognize adverse-event content and route it to pharmacovigilance.
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
Load the sources
Upload the reports, papers, and approved documents in scope.
- 02
Investigate
Use Stethos to summarize, compare, and surface open questions.
- 03
Draft for review
Produce plain-language output for the accountable reviewer.
- 04
Route regulated issues
Safety, quality, and promotional questions go to their owners.
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
- Individual Lab workspaces for evidence work
- File-aware Stethos conversations
- Saved investigations, notes, and sources per project
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 give prescribing advice?
No. Prescribing decisions require a qualified professional with the full patient context and current product information. Lunas helps professionals read, organize, and explain evidence — the clinical call is never the software's.
Can it automate adverse-event reporting?
No. Pharmacovigilance runs on validated processes with defined human responsibilities, and Lunas is not a reporting channel. Its useful role is upstream: helping a professional recognize and organize information before handing it to the safety team.
Can we restrict Stethos to our approved content?
Not in today's product — that control is core to the planned enterprise offering, which is why the current individual product shouldn't be treated as a validated pharmaceutical knowledge system. Today, professionals work with the documents they upload themselves.
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.