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QC 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.
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QC Workflows Configured Around Your Methods and Decision Rules

LIMS Parameter sets
Group tests into panels that match your QC processes and specs.
LIMS matrices
Define sample types based on your raw materials, batches, or products.
Calculated parameter quality control LIMS
Use formulas to track deviations, averages, or other key values.
Instruments in a Laboratory management software interface
Assign instruments and keep track of their usage in QC workflows.
QC LIMS analysis interface
Monitor how samples move through review and approval in your QA process.

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.

Odoo

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 15 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

Need Help?

FAQs

Yes. You can set your own test parameters, limits, and units for different products, materials, or workflows.

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.

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.

Yes. You can document out-of-spec results, classify nonconformities, assign corrective or preventive actions (CAPA), and track resolution status.

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.

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.

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