Designed around the way
your specialty works.
Medication order → clinical verification → preparation/dispensing → administration → monitoring.
Reconcile home and inpatient medicines; prescribe using ingredient, product, formulation, strength, route and schedule.
Pharmacist reviews allergies, duplicate therapy, interactions, renal/hepatic considerations and formulary restrictions using a maintained knowledge source.
Manage purchasing, batches, expiry, cold chain, controlled-drug accountability, partial dispensing, substitutions and returns.
Support eMAR, barcode checks, compounding worksheets and infusion plans; keep ordered, dispensed and administered quantities distinct.
Diagnosis coverage and clinical records
Pharmacy links each therapy to indication and patient conditions; tracks allergy versus intolerance, adverse drug reaction, medication error and adherence issues. It should not invent new diagnoses from an interaction alert.
Measurements that give the record meaning
| Measurement | Units / representation | Clinical context |
|---|---|---|
| Dose and strength | mg; microgram; units; mg/mL | Product-specific units and route |
| Weight/BSA-based calculation inputs | kg; m² | Verified date, formula and calculation version |
| Infusion rate | mL/h or drug-specific rate | Concentration, patient weight when applicable and pump library |
| Renal function | mL/min; mL/min/1.73m² | Named equation; indexed/non-indexed distinction |
| Inventory | packs; tablets; mL | Pack conversions and batch |
| Cold chain | °C | Device, excursion duration and disposition |
| Drug monitoring | assay-specific concentration | Collection relative to dose and clinical target source |
Equipment and integration plans
- Barcode scanners, dispensing cabinets, compounding systems and smart pumps → verification/dispensing/administration events via approved middleware.
- Pump auto-programming is a separate high-risk validated project; initial scope imports administration evidence and compares it to orders, without controlling infusion.
Connections require an approved interface and testing against the installed manufacturer, model and software. Listed equipment is a candidate integration target.
Explore equipment & roboticsReporting and meaningful outcomes
Dispensing turnaround, stockouts, expired stock, medication discrepancies and omitted doses with documented reasons; separate detected incidents from estimated clinical harm.
Development scope and clinical validation
Initial scope
Prescribing, pharmacist review, inventory, dispensing and administration records.
Advanced scope
Cabinet/pump integration, compounding and carefully validated decision support.
Example acceptance scenarios
- Microgram/milligram, concentration and pack conversions require explicit unit validation; reject ambiguous mappings.
- A scanned package is not proof that a dose was administered; cancelled/held doses remain visible in the eMAR.
Research foundations
Research snapshot: 23 September 2026. References inform the proposed design; they do not certify FertPro or establish device compatibility. Diagnosis lists and measurement groups are not treatment protocols.