Technologist and coordinator time wasted searching for and reconciling send‑out specimens
Definition
Poor send‑out tracking forces staff to spend substantial time locating specimens, checking multiple systems or calling reference labs, instead of performing testing or value‑added work. Sample tracking vendors emphasize that their systems eliminate manual transcription and time‑consuming searches and provide near‑100% visibility of specimen location, implying that such searching is currently a significant burden.[1][4][6][8]
Key Findings
- Financial Impact: 0.25–0.5 FTE per shift in many busy labs (tens of thousands of dollars annually) devoted to chasing send‑outs and reconciling logs vs. automated tracking; large reference labs report needing dedicated staff just to trace missing shipments before implementing advanced tracking
- Frequency: Daily
- Root Cause: Reliance on paper logbooks or disparate spreadsheets; no consolidated, searchable view of send‑out location and status; and lack of automated notifications when expected specimens are not received at the reference lab.[1][4][6][8]
Why This Matters
This pain point represents a significant opportunity for B2B solutions targeting Medical and Diagnostic Laboratories.
Affected Stakeholders
Medical technologists, Send‑out/reference lab coordinators, Phlebotomy staff, Lab supervisors
Deep Analysis (Premium)
Financial Impact
$10,000–$25,000 per year in staff time and lost productivity, plus revenue leakage from unbilled send-out orders when specimens cannot be accounted for or must be recollected at a later visit. • $10,000–$30,000 per year in wasted phlebotomist and coordinator time plus added redraw costs, patient dissatisfaction, and risk of uncompensated work when send-out specimens are lost before reaching the reference lab. • $15,000–$40,000 per year in analyst time and consultant costs, plus revenue risk if payers challenge claims, delay payments, or penalize the organization for missed turnaround commitments.
Current Workarounds
Ad hoc SQL queries or LIS reports, manual reconciliation of LIS order logs with courier exports and reference lab interface files, and creation of custom spreadsheets to track problem specimens and monitor turnaround time for send-outs. • Ad-hoc Excel exports from LIS and manual log matching • Cross-checking logs, phone calls to reference labs, and manual Excel reconciliation
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Methodology & Sources
Data collected via OSINT from regulatory filings, industry audits, and verified case studies.
Related Business Risks
Lost charge capture for send‑out tests due to poor tracking and order/result mismatches
Excess courier, shipping, and labor costs from inefficient send‑out specimen tracking
Lost, misrouted, or compromised send‑out specimens leading to redraws and repeat testing
Delayed billing and extended AR from slow send‑out status visibility
Chain-of-custody and traceability deficiencies risking CLIA/ISO nonconformities for send‑outs
Opportunity for inappropriate test billing and misuse of send‑out workflows due to weak tracking controls
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