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Built on Cloud. IntegratedRegulatory Standards21 CFR Part 11

LIMS Software for Laboratory Compliance & Data Management

Digitize your lab end-to-end. Sample registration, test execution, instrument capture, COA generation, stability studies, regulatory compliance. ERP integrated.

Built for QA heads, lab managers, and regulatory teams in pharma, chemicals, food, and manufacturing enterprises.

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LIMS Software
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100%
Audit Readiness
Zero
Paper Records
60%
Faster TAT
Auto
COA Release
Core Capabilities

Stop Risking Failed Audits and Recalled Batches. Digitize Your Lab.

Sample Registration

Register samples with customer, source, pricing, collection, and test plan details in a centralized workflow.

Test Management

Manage test methods, specifications, standards, result parameters, and built-in calculation logic.

Workflow Execution

Assign tasks, track analyst worklists, monitor delays, manage approvals, and control lab processes.

Equipment & Inventory

Manage test equipment, inventory, stock, retention samples, and operational resources.

Process Architecture

Lab Management Lifecycle Simplified & Digitized.

OptiLIMS Laboratory Lifecycle Diagram
End-to-End Workflow

Eliminate Paper Lab Notebooks and Spreadsheet Test Records.

01

Registration

Sample registered with batch, source, and test plan linked—no more paper notebooks.

02

Methods

Assign test methods per spec. Generate analyst worklists automatically.

03

Capture

Capture results from instruments or manual entry with strict validation.

04

Approval

Review results and trigger OOS investigations when deviations occur.

05

Batch Release

Auto-generate digitally signed COA and post usage decision to ERP.

All Sample Types

Every Sample Category. Centrally Managed.

💊

Pharma QC

QC/QA, ICH stability, and batch release.

🧪

Chemicals

Raw material and in-process checks.

🍎

Food/FMCG

Microbiological and nutritional analysis.

🏗️

Manufacturing

Metallurgical and incoming inspection.

Energy

Fuel, lubricant, and emissions testing.

🧵

Textiles

Fastness, tensile, and Oeko-Tex protocols.

Regulatory Standards

Built for regulated industries. Every standard.

21 CFR Part 11
ALCOA+ Principles
GAMP 5
ISO 17025
ICH Guidelines
GMP / GLP
Connected Integrations

Stop Re-Keying Lab Results. One Integrated Stack.

Stop running labs as a parallel universe outside ERP. OptiLIMS unifies lab operations by connecting with your core business systems.

Post usage decision and batch release
Automatic inspection lot closure
Direct instrument data capture
Centralized quality records hub
Built for Every Regulated Sector

Lab Management Tailored for Every Regulated Sector.

21 CFR Part 11

Pharma & Life Sciences

ICH stability, method validation, OOS, batch release, GMP, and 21 CFR Part 11 compliance.

ISO 17025

Chemicals & Petrochemicals

Raw material testing, in-process checks, COA generation, and ISO 17025 calibration.

FSSAI / HACCP

Food & Beverage

Microbiological testing, shelf-life studies, FSSAI compliance, and HACCP integration.

Get Your Questions Answered

Still Have LIMS Doubts Before You Decide?

Built for QA heads and lab managers evaluating LIMS.

Digitize your lab end-to-end to stop risking failed audits and recalled batches. OptiLIMS unifies lab operations with your ERP.

Still Running Lab Operations on Paper and Spreadsheets?

Stop running labs on paper and spreadsheets. See OptiLIMS digitize end-to-end. Enterprise lab management you can finally trust.