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