LIMS.SCIENCEQC LIMS for Batch Review, Control Charts and Nonconforming Work
Review analytical batches against predefined criteria, monitor the validity of results and control nonconforming work in one LIMS. Customer-configured workflows connect QC decisions to instruments, specifications, inventory, logistics, statistics and authorised result release.
QC Workflows Configured Around Your Methods and Decision Rules
The sector in practice · Industrial quality control
Two views of your laboratory workflow
Anonymous metal coupons linked to tensile properties, hardness and surface finish, with measurement-control traceability.
General examples shown for illustrative purposes.
AnalysesSamplesTechnical reviewReportLaboratory · Industrial quality control
Uniaxial tensile properties
IND-260903 · MET-IND-01 · UTM-IND-01
| Sample | Proof stress Rp0.2 MPa | Tensile strength MPa | Elongation at break % |
|---|---|---|---|
IND-001Aluminium alloy coupon | 285 | 335 | 12.4 |
IND-002Steel alloy coupon | 365 | 515 | 24.8 |
IND-003Copper alloy coupon | 210 | 345 | 32.6 |
UTM-IND-01Acquisition completeMET-IND-01
Result file linked to the batch
IND-260903 · 03/09/2026 · 15:20Illustrative interface · fictional data
Metal tensile-property review
Proof stress, tensile strength and elongation at break linked to the test machine and specimen identifiers.
Analytical report
RPT-IND-260903-01 · Version 1.0
| Parameter | Unit | I01 | I02 | I03 |
|---|---|---|---|---|
| Proof stress Rp0.2 | MPa | 285 | 365 | 210 |
| Tensile strength | MPa | 335 | 515 | 345 |
| Elongation at break | % | 12.4 | 24.8 | 32.6 |
| Vickers hardness | HV10 | 112 | 158 | 108 |
| Surface roughness Ra | µm | 0.82 | 0.45 | 0.68 |
I01 : IND-001I02 : IND-002I03 : IND-003
Units and result qualifiers preserved.
Illustrative results only; no regulatory conformity conclusion.
Authorised on 05/09/2026 at 09:00Technical manager · Version 1.0
IND-260903 · 05/09/2026 · 09:00Illustrative interface · fictional data
Mechanical results and measurement controls
Tensile properties, Vickers hardness and surface roughness compiled with the force-check record.
QC Parameters, QA Reports and LIMS Quality Management for Laboratory Compliance
Common QC Parameters
- pH
- Conductivity
- Moisture Content
- Viscosity
- Density
- Ash Content
- Tensile Strength
- Melting Point
- Colour (Visual / Spectrophotometric)
- Particle Size Distribution
- Microbial Load
- Contaminants (Pb, Hg, As, etc.)
- Residual Solvents
- Surface Roughness
- Odor / Appearance
- …etc.
QA & QC Reports
- Batch Quality Reports
- Calibration Certificates
- QC Summary Sheets
- COA (Certificate of Analysis)
- Internal Audit Reports
- Nonconformity Reports
- Corrective Action Logs
- Sample Receiving & Log Sheets
- Process Validation Records
- Trend & Deviation Analysis Charts
- Test Method Validation
- Product Release Forms
- Raw Data Entry Sheets
- Equipment Qualification Logs
- …etc.
Compliance Standards
- ISO/IEC 17025
- ISO 9001
- Applicable GMP requirements; OECD GLP controls where relevant to non-clinical health and environmental safety studies intended for regulatory submission
- FDA 21 CFR Part 11
- Internal SOP & QA Policies
- Customer-Specific QA Requirements
- Analyst Signature & Review Logs
- Traceability & Chain of Custody
- Method Validation Protocols
- Audit Readiness Requirements
- Retention & Record Control Policies
- Confidentiality & Data Integrity
- National / Industry-Specific Guidelines
- …etc.
QC LIMS Features for Industrial Quality Control and QA Labs
Our LIMS is purpose-built for quality control testing in laboratories. Whether you're managing pretreatment samples, auditing QA processes, or enforcing ISO standards, this QC LIMS provides tools to support controlled, traceable processes.
Logistics and Chain of Custody
Track raw materials, in-process samples and finished products through receipt, custody, preparation, storage and disposal. Configure sampling routes and acceptance states by product, site and programme.
Customer-Configured QC Workflows
Define roles, review gates, exception paths and release decisions for each product and method. Workflow versions, effective dates and approvals remain attributable under change control.
Analytics and Metrology
Bind authorised instruments to methods and capture results through suitable interfaces. Calibration status, reference standards and uncertainty records remain connected to the affected analytical work.
Monitor the Validity of Results
Evaluate blanks, spikes, duplicates, reference materials and control-chart limits against predefined criteria. Failed rules route the batch to authorised review and, where required, control of nonconforming work.
Statistics and Trend Review
Analyse results across methods, instruments, products, sites and time periods using trends, control limits and QC indicators. Controlled reports retain the reviewed data set, authorisation and applicable specification.
Inventory and Business Operations
Tie reagent and consumable lots to batches and methods, then connect approved laboratory records to procurement, production, billing and client operations through Odoo and scoped integrations.
LIMS Software for QA, QC and Lab Quality Control, Built on Odoo
Lims.science runs entirely on Odoo, a powerful ERP system trusted by over 28 million users across the world.
This LIMS supports industrial laboratories with defined QC workflows, method-validation records, QA review and processes aligned with ISO/IEC 17025 or ISO 9001.
- Configure test methods, limits, and units for industrial QA and QC needs
- Track sample flow, storage conditions, and test timelines across lab stages
- Approve or reject results with attributable, time-stamped change histories and deviation tracking
- Assign user roles so QA leads, lab staff, and clients access only what they need
- Manage multiple lab sites and processes from a single dashboard
- Access securely in the cloud or on your own servers
FAQs
Can I customise test methods and limits?
Yes. You can set your own test parameters, limits, and units for different products, materials, or workflows.
How does this LIMS support ISO 9001 or ISO/IEC 17025 requirements?
The LIMS provides configurable controls for approved procedures, analyst authorisation, metrological and sample traceability, attributable change histories and controlled reporting. These controls can support requirements relevant to the laboratory’s ISO/IEC 17025 accredited scope when implemented within its quality system.
Can multiple labs or plants use the same system?
Absolutely. The LIMS can be configured to manage multiple locations or departments in one centralised platform. Each site can have its own tests, users, and workflows, while management gets unified oversight through role-based dashboards and reports.
Does the system support tracking nonconformity and corrective actions?
Yes. You can document out-of-spec results, classify nonconformities, assign corrective or preventive actions (CAPA), and track resolution status.
Can I manage instrument calibration and maintenance schedules?
Yes. You can log calibration certificates, schedule future calibrations, and track equipment maintenance history. Alerts can be configured to notify you of upcoming due dates, supporting review of calibration status and suitability for the assigned method.
Can I export data or reports for audits?
Yes. You can generate and export reports in multiple formats (PDF, Excel, CSV), making audit prep quick and hassle-free.
QC LIMS That Makes Laboratory Quality Control Easier to Manage
Handle lab audits, QC reports, pretreatment tests, and compliance in one LIMS platform designed for quality control.