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ErgoLIMS for Chemical & Analytical Testing
31 methods · 15 instruments · 8 limits on day one

Whatever arrives, you can answer for the number.

A general analytical lab lives on the strength of a single figure on a certificate. ErgoLIMS holds the digestion batch, the calibration curve, the instrument that was in date, the analyst who was trained and the specification it was judged against — behind every one of them.

ISO/IEC 17025:2017
NABL
IS 3025
AOAC
ASTM

Ring structures — drawn live in the browser, no two frames alike

The problem

The number is easy. Defending it three months later is not.

A chemical lab runs the widest method list of any discipline and the narrowest customer specifications. The result sits in an instrument export, the dilution factor lives in a notebook, the specification came in an email, and the analyst who ran it has left. When the customer disputes the figure, reconstructing it is archaeology.

Instrument exports transcribed into a spreadsheet, then into a report — two chances to fumble a decimal place
Dilution factors and digestion batches recorded on paper that never reaches the certificate
Each customer has their own specification, and the analyst has to remember which limits apply
A lapsed AAS calibration discovered only when the certificate is already with the customer
Related-substance and residue methods with no place to hold the validation that justifies them
Two analysts, two rounding conventions, two different answers from the same raw data
What ErgoLIMS does about it

Six things a chemical lab gets that a spreadsheet cannot give it

Each of these is a shipped capability, not a roadmap item.

The calculation is part of the record

The formula, the dilution factor, the significant figures and the expanded uncertainty are applied when the result is saved, not afterwards in a spreadsheet. Every execution writes a log, so the arithmetic that produced the reported figure can be re-read years later.

The number on the certificate is reproducible from the record, not from memory.

A lapsed instrument stops producing results

AAS, ICP, GC and HPLC all carry a calibration due date. When one passes, the instrument stops being selectable for result entry — the block happens on the server, so it holds regardless of which screen or API call is used.

You find the lapse before the certificate goes out, not during the assessment.

Every customer’s specification, kept apart

Limits belong to the specification, not to the test. The same lead determination can be judged against a customer specification, an IS limit or a monograph, and the certificate records which one applied.

Pass or fail is decided by the specification on the job, not by the analyst’s recollection.

The analyst cannot approve their own work

Separation of duties is enforced server-side. The person who entered a result is refused when they try to approve it, and the reviewer sees the raw value, the calculation and the specification together rather than a bare number.

A second pair of eyes is structural, not a habit that slips when the lab is busy.

Digestion and extraction batches are traceable

Preparation references and dilution factors are captured at result entry, so a suspect digestion batch can be traced to every sample that went through it.

One bad batch means one recall list, produced in seconds.

Certificates a customer can verify

Every issued certificate carries a QR code that resolves to a verification page. A withdrawn certificate returns a clear gone response rather than continuing to verify.

A forged or superseded certificate fails the check the customer runs themselves.
End to end

How a chemical sample moves through the system

Receive and describe — The registration form — three steps, with the customer-committed date and the internal lab target kept as separate fields.

The registration form — three steps, with the customer-committed date and the internal lab target kept as separate fields.

Material descriptionPhysical formHazard classSpecification ref
Who it is for

Three people in the lab, three different wins

Analytical chemist

Enters the reading and gets the calculated result, correctly rounded, without opening a spreadsheet.

Quality manager

Can show an assessor the full chain behind any figure on any certificate, in the room.

Lab director

Sees which methods are drifting, which instruments are near their calibration date and where turnaround is slipping.

Built to be assessed

Compliance a chemical assessor will recognise

ISO/IEC 17025:2017

Method validation, uncertainty budgets, QC charts and the management-system records the standard asks for.

NABL

Atomic ULR allocation, accredited-scope handling and authorised signatory registers.

Audit trail

Who, when, old value, new value and reason on every controlled change, enforced by a database trigger.

Traceability

Reference material register with certificates and expiry, and instrument calibration lockout at the point of use.

And you do not start from an empty system

Choose the chemical domain at setup and ErgoLIMS provisions the scaffolding for you — as editable templates, not a locked configuration. The eight seeded limits are IS 1070 reagent-water values for the lab’s own QC — not product acceptance limits. General chemistry limits come from the customer specification, which is configured per product in the specification master.

6
Departments
31
Test methods
15
Instruments
8
Spec limits
Asked by labs like yours

Questions we hear from chemical labs

Yes. A method carries its own standard reference, units, decimal places and LOD/LOQ, so an AOAC method and an in-house SOP sit side by side and each reports the way it should.

See it run on your own parameters

A 30-minute walkthrough with the engineers who built it — using your methods, your limits and your reporting format, not a canned script.