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Pharma & LIMS Solution

Your entire lab. One platform.

From sample reception to client report, Yoddo Pharma replaces scattered spreadsheets with a unified LIMS + ERP that keeps you audit-ready at all times.

From sample to invoice in 5 steps.

1

Reception

Register samples, print barcodes, assign analysis plans.

2

Analysis

Capture results from instruments or manual entry.

3

Validation

Multi-level review with electronic signatures.

4

Report

Auto-generate branded client reports in PDF.

5

Invoice

Bill clients automatically based on completed analyses.

Module

LIMS — Laboratory Information Management

Centralize every analysis your lab performs. Register samples with unique barcodes, assign test methods, capture results from instruments or manually, and track every step with a complete audit trail.

Sample registration with barcode printing
Test method library with specifications and limits
Instrument data import (CSV, API, serial)
Out-of-spec alerts with automatic deviation creation
Worksheet management per analyst
Sample Lifecycle
Reception & Registration Auto-ID
Analysis & Testing In Progress
Review & Validation Pending
Report Generation PDF

Module

Quality Control & GMP Compliance

Enforce Good Manufacturing Practices at every stage. Define quality checkpoints, manage non-conformities, and ensure every product leaving your lab meets regulatory standards.

Quality control plans per product / client
Non-conformity reports with root cause analysis
CAPA (Corrective & Preventive Actions) tracking
Calibration schedules for instruments
SOP document management with version control
Compliance Dashboard
98.5%
Conformity Rate
3
Open CAPAs
12
Calibrations Due
0
Critical Deviations
ISO 17025 Compliant
GMP / BPF Ready

Module

Multi-Level Validation

Implement up to 4 levels of review before any result is finalized. Electronic signatures ensure accountability. Every validation is timestamped and logged in an immutable audit trail — exactly what auditors expect.

Configurable approval workflows (1 to 4 levels)
Electronic signatures with password confirmation
Reject with comments — analyst re-tests automatically
Immutable audit trail: who validated, when, what changed
Role-based permissions (Analyst, Reviewer, QA Manager)
Approval Chain
Analyst submits results Level 1
Reviewer validates data Level 2
QA Manager approves Level 3
Report released to client Final

Module

Batch & Lot Traceability

Track every batch from raw material procurement to finished product release. In case of a quality issue, perform instant upstream and downstream recalls with complete genealogy. Expiry date management included.

Lot/batch number assignment and tracking
Upstream traceability: raw material → supplier
Downstream traceability: batch → client deliveries
Expiry date tracking with automatic alerts
One-click product recall simulation
Batch Genealogy
Raw Material RM-2024-001 Supplier A
Production Batch PB-0423 In QC
Delivery to Client XYZ Shipped

Module

Stability Studies

Plan and execute ICH-compliant stability studies. Define storage conditions, sampling schedules, and test parameters. Track results over time and determine shelf life with confidence.

ICH Q1A/Q1B compliant study protocols
Automated pull-point scheduling (T0, T3, T6, T12...)
Chamber management (25°C/60% RH, 40°C/75% RH)
Trend analysis and shelf life determination
Automatic notifications for upcoming pull dates
Study Timeline
T0
Initial Testing
T3
3 Months
T6
6 Months
T12
12 Months
Long-term: 25°C ± 2°C / 60% ± 5% RH
Accelerated: 40°C ± 2°C / 75% ± 5% RH

Module

Environmental Monitoring

Monitor cleanroom conditions, water systems, and compressed gases. Define sampling points, frequencies, and alert/action limits. Detect trends before they become out-of-spec events.

Sampling point management with floor plans
Air viable & non-viable particle monitoring
Water system monitoring (WFI, PW, potable)
Alert and action limits with automatic escalation
Trend analysis with statistical control charts
Cleanroom Zones
A
Critical Zone
B
Background
C
Preparation
D
Support
Next sampling: Today 14:00 3 points
15M+
Odoo users worldwide
100%
Audit traceability
ISO
17025 ready
24/7
Cloud availability

Simple, transparent pricing.

Very Small

1 vCPU
2 GB RAM
1 GB SSD
5 DA/mo

Small

2 vCPU
4 GB RAM
1 GB SSD
50 DA/mo

Medium

4 vCPU
8 GB RAM
1 GB SSD
75 DA/mo

Big

8 vCPU
16 GB RAM
1 GB SSD
100 DA/mo
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