Your numbers,
before you call.
Configure your specimen workflow. Turnaround hours, cost per case, and compliance score update in real time on the right.
No commitment · Assessment in 24 hours · HIPAA-compliant
Estimates are based on standard workflow parameters and current lab capacity. Final pricing confirmed upon specimen submission and protocol review.
Accreditation
without asterisks.
Every badge on this page links to a verifiable certificate. We operate under three independent accreditation bodies — not because compliance requires it, but because our clients' results demand it.
College of American Pathologists
Biennial on-site inspection covering 2,800+ checklist items across pre-analytic, analytic, and post-analytic phases. Proficiency testing in 42 analyte categories.
- Slide preparation & staining QC
- Reagent lot-to-lot validation
- Pathologist credentialing audit
- PT result submission within 30 days
Clinical Laboratory Improvement Amendments
Federal certificate covering all human specimen testing. Encompasses personnel qualifications, QC procedures, proficiency testing, and patient test management.
- High-complexity testing certificate
- Director qualification on file
- Daily QC documentation
- Test system validation records
Medical Laboratories — Requirements for Quality & Competence
International standard specifying quality management and technical competence requirements. Covers measurement uncertainty, traceability, and pre-examination processes.
- Risk management framework (ISO 22367)
- Measurement uncertainty budgets
- Reference interval verification
- Complaint & nonconformity tracking
Chain of
custody.
From arrival dock to signed report — every hand-off logged, timestamped, and auditable within 30 seconds.
Specimen Receipt & Accessioning
Barcode-scanned within 15 min of arrival. Condition assessed against submission form. Discrepancies trigger immediate client notification via LIS alert.
Automated Tissue Processing
Leica ASP300S tissue processor. Overnight cycle for FFPE; rapid 4-hour protocol available for STAT cases. Temperature and reagent logs archived for 10 years.
Staining & Coverslipping
Automated H&E and special stain platforms. IHC panels on Leica Bond-RX with positive and negative controls on every run. Digital scan triggers QC check before pathologist review.
Gross Examination & Cassetting
Pathologist assistant performs gross description per CAP protocol. Tissue sections selected, labeled with unique cassette ID, and routed to processing queue.
Embedding & Sectioning
Paraffin embedding at 60°C. Microtome sections at 3–5 µm. Section quality reviewed before staining — warped or compressed sections re-cut automatically.
Pathologist Sign-Out & Report
Board-certified pathologist review. Final report delivered to LIS within SLA window. Addenda tracked with timestamp. Second-opinion escalation available within 4 hours.
Staining
consistency.
Drag the divider to compare raw vs. optimized staining. Every run includes calibration standards — deviation triggers immediate re-run, not a workaround.
Uneven hematoxylin — nuclear detail obscured
Crisp nuclear detail — mitotic figures countable
Digital
pathology.
Whole-slide imaging at 0.25 µm/pixel. Every slide scanned, annotated, and delivered to your existing LIS — no workflow disruption, no new software to install.
Click annotation markers above to view pathologist notes. All annotations are embedded in the HL7/FHIR report and synchronized to your LIS within 60 seconds of sign-out.
LIS / LIMS Compatibility
Native integration = direct HL7/FHIR feed. API = REST endpoint with full documentation.
Don't see your platform? Our integration team configures custom HL7 mappings in 3–5 business days. No middleware required.
Get Your
Lab Assessment.
A board-certified pathologist and lab operations consultant review your current workflow and return a written assessment within 24 hours.
Specimen Submission Guide
Complete prep protocol: fixation times, labeling requirements, shipping conditions, and rejection criteria for all specimen types.