Flexible endoscope reprocessing runs a dozen exacting steps, dozens of times a day, where a single miss is a patient-safety event. ClarityComply guides every HLD step, documents each one, and ties every scope to the patient — under AAMI ST91.
Flexible endoscopes have been at the center of the most serious reprocessing-linked infection events in modern healthcare, and surveyors know it. The workflow is long, manual, and repetitive, and every step has to happen in order, every time. A skipped leak test, a short soak, an un-brushed channel — any one of them can turn a routine case into a patient-safety and liability event. Manual checklists weren't built to carry that.
ClarityComply walks the technician through the full ST91 reprocessing chain — no step skippable, each one recorded as it's completed.
Not steam sterilization with the labels changed — HLD reprocessing guided and documented on its own terms.
Bedside pre-clean through storage, enforced in order and cited to ST91 and your scope IFUs — with soak time and MEC checks built in.
Every reprocessing cycle ties a specific scope to the case it served. If a failure surfaces, you can identify every affected patient — fast.
Each cycle becomes an attributed, timestamped record. When a surveyor asks how scope EC-1187 was reprocessed, the answer already exists.
The nightmare scenario in endoscopy isn't just a reprocessing miss — it's discovering one and not knowing which patients were exposed. ClarityComply keeps a hard link from every scope, through every reprocessing cycle, to every case — so a recall is a query, not a forensic reconstruction.
See the GI/HLD Event Library →Configured to your scope inventory, your AER, and your volume.
Independent centers running high volumes on lean staffing.
Higher scope counts and shift coverage. See Facility →
Office-based scope reprocessing with survey obligations.
Independent GI centers start on Practice. Hospital-based endoscopy departments deploy through Facility.
Self-serve, same-day, priced by procedure volume — with a 30-day pilot on your real scope reprocessing that credits toward month one.
The full decision layer for a hospital endoscopy department — scoped in a working session with your scope inventory, AER, and existing systems.
Built for HLD specifically. GI/endoscopy is one of the platform's core event categories, with flows that follow the ST91 reprocessing chain — bedside pre-clean, leak test, manual cleaning, high-level disinfection with soak-time and MEC checks, drying, and storage — not a steam-sterilization workflow relabeled.
Each scope is tracked as a unique instrument. Every reprocessing cycle is documented against it, and it's linked to the patient case it served. If a reprocessing failure is ever identified, you can pull every case a given scope touched in seconds — the difference between a targeted recall and a forensic reconstruction.
The guided flow works alongside your AER out of the gate — it structures the manual steps around it and captures the cycle. Direct equipment integrations live at the Connected tier and are scoped to your setup; you don't need them to start documenting correctly. See the tiers.
Not at all — many endoscopy settings don't, and ClarityComply stands on its own as your reprocessing standard. If you do run something, it sits on top. Either way you get guided steps, documentation, and traceability from day one. Overlay or standalone.
That's the point of it. Every cycle produces a contemporaneous, attributed, ST91-cited record — including soak time, MEC, and traceability — generated as reprocessing happens. When a surveyor drills into scope reprocessing, you hand them the record instead of rebuilding it. See how a guided event documents itself.
Start a 30-day pilot on your real scope reprocessing, or see the guided HLD flow run in a short walkthrough.