Blood bank SOP intelligence for transfusion services · In development
Your procedures, in force.
LMOS gives your blood bank cited answers from your approved SOPs and nothing else, then keeps document control, competency and CAP inspection readiness in step with them. Nothing changes without a signature.
Hold the unit and complete the antibody identification panel before crossmatch.
Answers come from your signed, in-force documents. No web, no guessing.
Each answer points to the exact passage, so anyone can check it in seconds.
Changes to procedures go through a two-person sign-off with an audit trail.
Cited answers from your SOPs
An answer at the bench in seconds, with the receipt attached.
Techs ask in plain words. LMOS finds the passage in the approved procedure, quotes it, and says when no procedure covers the question instead of making one up.
Try a question. These use sample procedures, not clinical guidance.
Per the procedure: hold the unit, complete the antibody identification panel before crossmatch, and select antigen-negative units once the antibody is identified.
Built for transfusion services
Made for the transfusion service, not every lab at once.
Typing, antibody workups, crossmatch, product handling, emergency release. LMOS is built around transfusion-service work and the standards it answers to: the CAP Transfusion Medicine checklist, AABB Standards for Blood Banks and Transfusion Services, CLIA and FDA requirements.
It is designed to hold no patient data. It works on your procedures, training and quality records, never on a patient chart.
Agents with limits
Agents do the paperwork. People sign.
When a standard changes, LMOS is designed to find every procedure it touches, draft the redline, and route it for review. Credential expiries, competency due dates and read-and-acknowledge reminders get chased without anyone keeping a spreadsheet.
How LMOS differs
Most compliance AI writes your procedures. LMOS makes sure the bench follows them.
Generative tools draft policies from a prompt. LMOS starts from the procedures your director already signed and never goes beyond them.
| Question | Typical compliance AI | LMOS |
|---|---|---|
| What the AI does | Drafts policies and forms from prompts | Answers only from approved, in-force SOPs |
| Every answer shows | Generated text | The section and revision it came from |
| When no SOP covers it | Writes something plausible | Says so and flags the gap to quality |
| Who it serves | The quality office | The bench tech and the quality office |
| Built for | Every regulated lab at once | Transfusion services |
Modular by design
A small core. Modules for what you need.
Document control, read and acknowledge, competency assessment and CAP inspection readiness, built around the blood bank. The core holds grounding, signatures, audit trail and access control. Everything else is a module you turn on when you are ready.
Ask, Read and Acknowledge, Procedure Guide
The answer and the proof that staff read the current revision.
Designed to support CAP GEN.20375 · CLIA 42 CFR 493.1251Regulatory Intelligence, Inspection Readiness
Know which procedures a change touches before the inspector does.
Designed to support CAP TRM and GEN checklist preparationTraining, Competency, Roster and Credentials
Six-element competency and credential expiry, kept in order.
Designed to support CAP GEN.55500 and GEN.54400 · CLIA 42 CFR 493.1235Deviation and CAPA, Proficiency Testing, Vendors
Events, corrective actions and suppliers tied back to the SOP.
Designed to support CLIA 42 CFR 493.1239 and Subpart HRequirement references show what modules are designed to support. They are not certifications or accreditation decisions.
Trust and status
What is true today, and what is not yet.
We say where each item stands. Nothing is described as certified or validated until the document exists.
Pilot program
Help shape the first cohort.
We are forming the first pilot cohort of transfusion services. Tell us about your lab and what would help most.
Register for the pilot