Drop your instrument export
Parse every sample, analyte, and standard. No schema fiddling, no CSV cleanup.
One workflow for wavelength selection, CRM validation, and dilution math — so every run leaves the lab the same way.
The Laboratory
Scroll through the bench at Kimiya Pazhouh Alborz Laboratory. Every photograph here is a shared surface between the analyst and the software.

From the plasma torch to the detector, optical path calibration and alignment are part of the contract. We read your instrument's exported spectra line by line and preserve the analytical provenance all the way to your supplement.

Real analytical hardware punishes ad-hoc workflows. Dilution drifts, line choices compound, spreadsheets disagree. PreciseICP freezes each decision the instant it is made, so your final table matches the bench two years from now.

We built the interactions by watching how real analysts move through CRM validation, wavelength review, and QC. No hidden macros, no reformatting, no ambiguity about which dilution factor applies to which sample.
The Workflow
Parse every sample, analyte, and standard. No schema fiddling, no CSV cleanup.
Every analytical line is scored against your reference materials. We document the rationale.
CRMs, blanks, spikes, and checks flagged against your own limits. Out-of-range flags carry context.
Export structured tables with a traceable decision log for methods files, LIMS, or your supplement.
Why PreciseICP
0+
Elements per run, auto-validated
0k
Sample rows processed monthly
0.0%
Average CRM recovery target window
< 0s
Re-run delay from decision log
CRM-first
Wavelength decisions anchored to reference material performance
Structured QC
Checks, recoveries, and documented limits on every run
Smart dilutions
Factors applied once, concentration roll-up handled for you
Clean exports
Tables ready for methods files, peer review, and LIMS handoff
Recognition
Khwarizmi International Festival
First place, laboratory analysis software
National Elite Foundation
Innovation Award in Laboratory Technology
Iranian Analytical Chemistry Olympiad
Gold medal, analytical software category
Best Laboratory Software Award
Chemical Society of Iran, editors' choice
Capabilities
Every line is scored against your CRM data. The platform picks the one that holds up, and documents why.
CRMs, check standards, blanks, and spikes — checked against your thresholds. Recoveries calculated automatically; out-of-range results flagged with full context.
Dilution factors go in once. Concentrations roll up correctly across the batch — no copy-paste errors, no mismatched factors.
Bench to deliverable
Upload your run files, work through structured QC with full context, then freeze your concentrations before they leave the lab.
Step 1
Drop in your ICP-OES export; we parse every analyte, intensity, and standard.
Step 2
The platform evaluates each line against your own reference materials and documents the decision.
Step 3
CRMs, blanks, spikes, and check standards are flagged against your pass/fail limits.
Step 4
Export publication-ready tables with a traceable decision log, ready for methods files and LIMS.
Approach
CRM and control results drive wavelength validity and QC flags — conclusions follow data you trust, not a black box.
CRM spectrum · Cu 324.754 nm
Same inputs, same outputs, every time. Calculation context is preserved so decisions stay defensible weeks later.
Structured tables and QC summaries that drop straight into methods files, validation packages, and manuscript supplements.

Researcher feedback
Notes from university and contract labs in Iran and the region.
“Our last paper came back with only minor comments: the wavelength table in the supplement finally matched what we actually ran, because line picks and QC flags sit with the raw intensities instead of living in three different spreadsheet tabs.”
Dr. Maryam Hosseini
Environmental Geochemistry Laboratory, University of Tehran
Our last paper came back with only minor comments: the wavelength table in the supplement finally matched what we actually ran, because line picks and QC flags sit with the raw intensities instead of living in three different spreadsheet tabs.
I teach QA the same way we run the bench: CRM first, then everything else. The workflow bakes that in, so I am not reconciling three MSc students’ ad hoc wavelength edits at 9 p.m. the night before a deadline.
Queue-wise we never run one grant at a time: digestions for ceramics one week, brines the next. One processing template means I do not have to remember which Excel macro belonged to which PI.
We split time between contract digestions for upstream partners and our own R&D. Parallel workbooks still disagreed on the “official” dilution factor; a single workspace stopped those threads before they hit email.
My thesis chapter on soil trace metals had to show every dilution, rerun, and flag. Exporting the calculation log turned a two-day scramble before the committee into an afternoon of checking footnotes.
We hold an ISO/IEC 17025 scope for wear metals in lubricants. Auditors want the QC story in tables, not screenshots. Last surveillance audit, the structured run records dropped straight into our validation binder.
University labs, core facilities, and method-development groups running multi-element ICP-OES with formal QC and documentation needs. Particularly useful where multiple operators share one instrument.
Every available line is scored against your CRM and method criteria. The recommended line comes with rationale tied to those controls.
CRM, check standards, blanks, and spikes — with full recovery and limit evaluation. Out-of-range conditions are flagged with traceable criteria.
See the Plans page for tiers and payment options. Academic and institutional arrangements are available — reach out via Contact for facility licensing or a demo with your own data.
Have a compatibility or procurement question? Contact usPlans
Compatibility questions, demos, and institutional purchasing.
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