EKLIS.CLIENT REPORT
F-01 · STAFF

Staff, roles & competency

User management in a clinical lab is a compliance system, not an admin screen: CLIA defines who may test, who may supervise, and how competency is proven. Benchmark research (2026-09): LABGEN publishes almost nothing here — labs bolt on platforms like MediaLab/Vastian for competency. EKLIS builds it in.

What the benchmark ships

LABGEN / MEDFAR

Thin public spec

"Robust security," login & reporting features, role-scoped portal users, e-signature via tablet/signature pad, staff training as a paid service. No published competency, credential, or CLIA-personnel module.

FIELD PRACTICE

Competency lives outside the LIS

Labs run MediaLab/Vastian (CAP Competency Assessment Hub: CLIA-compliant assessments, instrument checklists, automated scheduling, observer signatures) as a separate subscription next to their LIS.

BEST-IN-CLASS

Granular permissions

Dendi gates every configuration surface behind fine-grained permissions (e.g. a dedicated "Tests = Manage" right to edit order-entry questions); Orchard/Clinisys lead with audit trails.

Whitespace: native CLIA competency tracking inside the LIS is one of the two clearest differentiation gaps our research found. EKLIS ships it as part of the platform, not a second subscription.

EKLIS specification

GroupFeaturesPhase
Roles & accessFine-grained RBAC per module, function, and test · lab roles mapped to CLIA personnel categories (Lab Director, Technical Supervisor, Clinical Consultant, General Supervisor, Testing Personnel) with per-test authorization lists · deny by default · user deactivation preserves full audit history · last-admin lockout protectionP1
SecurityMFA · password policy · session timeout · per-interface machine credentials · per-user activity viewer (who viewed/edited which patient data, when) · e-signatures on result release and document approvalP1–P2
Credentials & licensesCredential/license registry (state license, certifications, degrees) with expiry alerts and document storage · signature-authority records signed by the directorP3
Competency (CLIA six elements)Tracked assessments for: direct observation of test performance · monitoring of result recording/reporting · review of intermediate results, QC, PT and maintenance records · direct observation of instrument maintenance · blind-sample testing · problem-solving assessment. Scheduling: initial, 6-month, then annual — with due lists and assessor-qualification enforcement (only qualified supervisors may assess testing personnel)P4 · compliance pack
TrainingTraining records · read-and-acknowledge SOP sign-off with versioned documentsP4
ProductivityTests verified per technologist, accession counts per operator, auto-verification vs manual-review share (feeds the Statistics page)P3
42 CFR 493 Subpart M — personnel§493.1413 / §493.1451 — six competency elementsHIPAA §164.312 — unique IDs, access & audit controlsCAP GEN — training & signature records