Guided study setup
Instrument and assay selections stay linked. The laboratory confirms the current IFU, study protocol and local limits before interpretation.
Private pilot
A local validation engine for laboratories that need more than a workbook.
AssayIQ Local Lab Edition turns structured chemistry validation data into consistent calculations, visual analysis and review-ready reports on Windows and macOS. The production application stays private and is installed only for licensed pilot laboratories.
Local by design
Keep control of the data. Standardize the work.
Laboratories can use the public demonstration to evaluate the workflow. Licensed users receive a separate desktop application with local report export, controlled configuration and implementation support. Patient identifiers are not required for validation analysis.
ASSAYIQ LOCAL LAB EDITION
Installed for your laboratory
WindowsmacOS
- No public installer
- Local study storage
- Licensed PDF export
- Pilot onboarding included
Phase 1 release scope
Built around the real validation workflow.
The pilot moves the working engine beyond Excel while preserving transparent calculations, visible criteria and qualified review. The shared catalog includes all 70 quantitative CLIA routine chemistry, endocrinology and toxicology entries, grouped across chemistry, immunoassay and integrated instrument configurations. Manufacturer availability and ranges require local IFU confirmation; specialized methods have separate configurations.
Local-first data handling
Study files remain on the laboratory computer or approved local network location. The pilot does not require routine cloud upload.
Review-ready report packages
Generate a consistent report with study inputs, calculations, acceptance criteria, charts, findings and approval fields.
Quality controls built into the workflow
Required fields, version details and review checkpoints reduce missing documentation without replacing technical judgment.
Included in the pilot build
- Linearity and analytical measurement range studies
- Method and instrument comparison workflows
- OLS and Deming regression views where appropriate
- Identity line, fitted line, bias table and configured acceptance limits
- Manufacturer range confirmation and local SOP criteria
- Controlled PDF output with reviewer and laboratory-director approval fields
- Local project files, backups and organization-specific report branding
- Windows 10/11 and current macOS support during the private pilot
Product modules
Select the workflow that matches the study.
Available modules are labeled separately from professional services so laboratories can see what the software currently performs and what requires a managed engagement.
Linearity / AMR
Assigned-versus-observed results, AMR coverage, regression, bias, recovery, charts and controlled approval fields.
Test this workflowMethod comparison
Comparator and candidate results with OLS, Deming, bias review, clinical interval context and documented exclusions.
Test this workflowCombined package
A coordinated package that keeps the linearity dataset and patient-sample comparison dataset separate and traceable.
Test this workflowEMI / dilution verification
Preview corrected dilution results, replicate summaries and an attached worksheet. The shared web/local calculation module is a pilot, not independently validated production software. Managed studies are scoped separately.
Test the EMI pilotWhy laboratories invest
You are not paying $7,500 for a regression equation.
You are paying for the system around the result: guided setup, laboratory-specific controls, consistent analysis, controlled reporting, local ownership, implementation and ongoing support. A lower-cost statistics package may calculate slope and bias, but the laboratory can still be left to design and maintain the rest of the validation process.
Built for the laboratory workflow
AssayIQ connects the instrument, assay, manufacturer range, acceptance criteria, study data, analysis and approvals in one guided process.
A complete report, not disconnected output
Results, charts, criteria, findings, limitations and signature fields are organized into a consistent review-ready package.
Local control of study data
The licensed application runs on approved Windows and macOS computers, allowing the laboratory to retain study files within its own environment.
Implementation is part of the purchase
The laboratory receives configuration, report branding, user setup, training and an implementation verification checklist, not simply a license key.
Less reinvention between studies
Reusable workflows and controlled updates reduce the need to rebuild formulas, charts, report language and approval sections for every assay.
Support that understands the work
Maintenance covers routine releases, supported assay-library updates, issue resolution and an annual configuration review.
What the laboratory needsLower-cost calculation toolAssayIQ Local Lab Edition
Statistical calculations and chartsOften includedIncluded in the guided workflow
Instrument and assay guardrailsLaboratory may configure separatelyLinked selections with confirmation steps
CLIA reference and local SOP criteriaLaboratory may add manuallyRecorded with the study
Complete technical reportOften assembled separatelyGenerated from the same study record
Approval and review structureOften maintained in local templatesBuilt into the report package
Installation, configuration and trainingVaries by productDefined implementation service
Local ownership and recurring supportVaries by productDefined license and maintenance terms
The practical difference
Evaluate the fit A cheaper product can be the right choice for a statistician who only needs calculations. AssayIQ is designed for laboratories that want a repeatable validation process and a director-ready record without building the operating system themselves.
Private-pilot pricing
Separate the license, implementation and long-term care.
Public pricing provides a planning baseline. A final proposal defines the number of users, workstations, sites, instrument configurations, training and any requested integrations.
One laboratory site, up to three named users and two activated computers. Includes the current Phase 1 chemistry modules.
Configuration, report branding, user setup, remote training and an implementation verification checklist.
Routine software updates, supported assay-library releases, issue resolution and annual configuration review.
First-year pilot investment starts at $10,000.
Year-one maintenance is included. Multi-site licensing, custom interfaces, data migration, onsite work and accelerated assay-library development are quoted separately.
Separate custom product
Your instrument is not listed? We can build the system around it.
AssayIQ can develop a dedicated local validation application for an unlisted analyzer, specialty platform or defined testing program. This is a ground-up software engagement, not simply the addition of an instrument name to a menu.
Request a custom-build assessmentCUSTOM INSTRUMENT SOFTWARE BUILDFrom $15,000Defined instrument platform and initial assay scope
Implementation and validation supportFrom $3,500
Updates and maintenanceFrom $3,000 / year
Discovery and technical scope
Define the instrument, assay menu, study types, users, operating environment, report requirements and any approved data-import needs.
Instrument and assay configuration
Build the controlled library from current manufacturer documents supplied or approved by the client, including methods, units, analytical ranges and required confirmation steps.
Analysis and reporting workflow
Configure appropriate statistics, acceptance-rule capture, charts, findings, limitations and organization-specific review and approval fields.
Testing and implementation
Complete calculation checks, user-acceptance testing, installation, training and an implementation evidence package for the laboratory's own approval process.
Custom means controlled. Final scope and pricing depend on the number of assays, method complexity, data interfaces, report requirements, sites and support level. The client remains responsible for confirming current manufacturer claims and approving intended use.
Public demo versus licensed software
Evaluate the workflow without exposing the product.
CapabilityWebsite demoLocal Lab Edition
Synthetic data entryYesYes
Watermarked report previewYesOptional
Report download and printingNoYes
Local project savingNoYes
Organization configurationNoYes
Installation and trainingNoIncluded
Routine updates and supportNoMaintenance plan
Software supports the quality system. It does not replace it.
Each laboratory remains responsible for validating the software in its environment, approving protocols and acceptance criteria, confirming current manufacturer claims, protecting data, reviewing calculations and authorizing final use. AssayIQ provides implementation evidence and training to support that process.
Request pilot scoping