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Oasis-LIMS (Laboratory Information Management System)

Sample-to-release tracking, instrument integration & audit-ready compliance.

01

OasisLIMS 4.0 Enterprise

Custom Solutions for Large Labs & R&D Centers

OasisLIMS
OasisLIMS
A pre-validated, 100% web-based LIMS engineered for large pharmaceutical and enterprise laboratories — automating the full sample lifecycle through deep instrument integration and built-in quality systems, compliant with 21 CFR Part 11, MHRA, GAMP, ISO 17025, PIC/S guidelines, and EU GMP standards.
Integrated Add-On Modules

Sample Lifecycle

End-to-end tracking from receipt to disposal.

Batch Management

Multi-batch release with quality decisions & review.

OOS / OOT Investigation

Structured workflow for out-of-spec deviations.

Instrument Integration

Real-time capture via O-Link middleware.

Inventory & Consumables

Reagents, standards & consumables with alerts.

e-Signatures & ELN

21 CFR Part 11 compliant electronic lab notebook.

Web-Based & Client/Server

Fully web-based and client/server enterprise platform with e-Worksheet — paperless worksheets for LIMS.

02

Oasis-LIMS Professional

Ideal for Small & Mid-Size Laboratories

A web-based and client/server LIMS for small to mid-size labs in pharma, chemicals, petro, and textiles — eliminating manual errors with automatic test calculations, CoA generation, and standardised analytical workflows, with no complex IT overhead.
Integrated Add-On Modules

Sample Management

Login, tracking & lifecycle per sample category.

Dynamic Worksheets

Auto-generated analytical work records & protocols.

LOD / Assay Calculations

Automated HPLC, GC & method-specific computations.

CoA Generation

Pharmacopoeial format with auto pass/fail decisions.

Inventory Control

Reagents & standards with low-stock alerts.

Audit & Security

Role-based access with comprehensive audit trail.

03

LIMZ-RD

LIMS for Pharma Product Development & R&D Labs

Purpose-built for R&D pharmaceutical labs engaged in new drug development — formulation, API characterisation, stability studies, method validation, and dissolution profiling. GLP and 21 CFR Part 11 compliant, with full project and protocol management for regulatory submissions.
Key Capabilities
01GLP Compliant 02Project Management 03Method Validation 04Online Trending 05Regulatory Ready

Project Management

Timelines, protocols & milestones for drug development.

API & Formulation

Characterisation data with version-controlled methods.

Dissolution Profiling

Multi-point profile capture & batch comparison.

Data Retrieval

Structured export for regulatory submissions & patents.

Barcode Labels

Auto-generated sample labels with unique IDs.

Access & Security

Role-based permissions with full audit trail.

Innovator Sample Management

Innovator (RLD) batch data benchmarked against R&D formulations for equivalence.

Web-Based & Client/Server

Fully web-based and client/server enterprise platform with e-Worksheet — paperless worksheets for LIMS.

04

True LIMZ CTL

Commercial Testing Labs with Integrated Billing

A complete LIMS for commercial and public testing labs — from sample receipt to disposal with a fully integrated billing engine that auto-applies contract pricing, discounts, and client-specific rules, turning lab data into accurate invoices with zero manual effort.
Key Capabilities
01Integrated Billing 02Contract Pricing 03Auto CoA 04Retention Samples 05Multi-lab Support

Party Rate Cards

Per-client rates auto-applied during billing.

Bill Processing

Sample-based billing with custom tax & numbering.

Payment Receipts

Payment tracking, search & amendment workflows.

Outstanding Statements

Due-amount views with full client ledger.

Sample Tracking

Receipt → testing → CoA → invoice, fully tracked.

Export Reports

Excel, PDF & HTML exports for all report types.

05

Stabi-M

Stability Data & Studies Management Software

ICH-compliant software for scheduling and managing complete stability programmes across multiple storage conditions, packaging types, and batch configurations — with regression analysis, statistical shelf-life prediction, and OOS/OOT alerting. Deployable standalone or integrated with OasisLIMS.
Key Capabilities
01ICH Guidelines 02Protocol Design 03Chamber Management 04OOS / OOT Alerts 05Statistical Regression

Protocol Design

Flexible setups with conditions, intervals & batches.

Chamber Management

Inventory & condition tracking across chambers.

Sample Pull Reminders

Dashboard alerts for upcoming pulls & withdrawals.

Trending & Graphs

Stability data plotted across time & conditions.

Statistical Analysis

Regression with shelf-life & expiry modelling.

OasisLIMS Integration

Seamless add-on to existing OasisLIMS installs.

Extend Your Platform

Want to know more about LIMS Add-On Modules?

EMS, EWM, Electronic Batch Records, Clinical Trials & more — modules that snap straight into your Integrated LIMS.