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.

• Sample traceability
• Identity & purity
• Instrument data
• Controlled COA

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

1. 01Agree the scopeDefine the sample, requested service and suitable method.
2. 02ReceiveReconcile vials, lot references, condition and custody.
3. 03PrepareRecord preparation and the controlled method used.
4. 04AnalyseLink instrument exports, evidence and structured results.
5. 05ReviewRecord technical decisions and resolve exceptions.
6. 06Issue the COARelease 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.