LIMS for peptide laboratories
Peptide analysis, from sample to controlled COA
Manage peptide samples, instrument imports, identity, purity and quantitative results in one Odoo-based LIMS. Keep the analytical record connected to technical review and controlled certificates of analysis.
A populated analysis view brings expected and observed mass, chromatographic purity, quantity and review conclusions into the same result table.
Retention time, peak area, area percentage, signal-to-noise and m/z remain visible for technical review. Importing a file does not approve its scientific interpretation.
Synthetic chromatogram and ESI mass spectrum with annotated peaks, charge states and an isotope-envelope detail.
General examples for illustration. Cropped screenshots from a UAT environment; customer details are excluded. Original interface: English. The displayed data are not analytical certificates. Illustration · synthetic data.
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One connected sample-to-report workflow
- Agree the scope
Define the sample, requested service and suitable method.
- Receive
Reconcile vials, lot references, condition and custody.
- Prepare
Record preparation and the controlled method used.
- Analyse
Link instrument exports, evidence and structured results.
- Review
Record technical decisions and resolve exceptions.
- Issue the COA
Release a versioned report with traceable supporting records.
Analytical data
- Expected and observed mass / m/z
- Chromatographic purity and quantitative result fields
- Retention times, peak areas and signal-to-noise
- Chromatogram and mass-spectrum evidence records
- Result units and decision rules configured by method
Controlled laboratory work
- Vial, lot and retained-sample traceability
- Sample suitability and preparation records
- Unexpected identity, holds and suitable-method retests
- Instrument file review and source-file hashes
- Attributable first and second technical validation
Reports and traceability
- Controlled certificates of analysis (COAs)
- Versioned reports and controlled reissues
- Frozen report snapshots and evidence appendices
- Audit history and sample custody events
- Commercial clearance separate from technical approval
Configured for your laboratory’s methods
The workflow is configured around your services, instruments, units, specifications and review responsibilities. The laboratory remains responsible for method suitability, scientific interpretation and authorised results.