Quality Control Laboratory
Testing Laboratory & Quality Assurance
Independent quality lab with ISO 9001 processes —every batch tested before shipment
Agrospear operates a dedicated quality control laboratory that operates independently from production. Every batch of raw material and every finished agrochemical formulation passes through documented inspection protocols before release. Our QC team reports directly to management, ensuring impartial quality decisions.
- 100%
- Batches tested
- Every raw material, every finished product
- 14 d
- Accelerated stability test duration
- At 54 °C per CIPAC MT 46
- ±2%
- Max active content deviation
- Over specification range
- AQL 2.5
- Major defect threshold
- Per ISO 2859 sampling
Raw Material Inspection
Every incoming batch of active ingredient, solvent, surfactant, adjuvant, and packaging component is tested before acceptance. Active content by HPLC/GC, moisture, particle size, pH, and identity confirmation are verified. Non-conforming materials are quarantined and returned.
In-Process QC Checkpoints
Production operators perform self-inspection at each stage. QC auditors conduct random sampling throughout the shift. Active content checks are performed after compounding. Particle size and viscosity checks happen after milling. Fill weight and torque verification after filling.
54 °C Accelerated Stability Test
Every formulation batch is held at 54 °C for 14 days per CIPAC MT 46. Active content, suspensibility, emulsion stability, pH, and appearance are tested before and after. Any batch showing sedimentation, phase separation, or active content degradation beyond tolerance triggers automatic batch re-inspection.
Final Specification Verification
Completed formulations are tested against the full project specification — active content, suspensibility, emulsion stability, pH, viscosity, particle size, and appearance. Each batch undergoes complete analytical verification before final inspection approval.
| HPLC System (active content) | UV/DAD detector, validated methods per CIPAC |
| GC System (volatile AI) | FID/ECD detector, headspace capability |
| Stability Chamber | 54 °C ±2 °C, CIPAC MT 46 compliant |
| Particle Size Analyzer (laser diffraction) | 0.01–3,500 µm range |
| pH Meter (calibrated) | ±0.01 resolution, temperature compensated |
| Viscometer (rotational) | 0.3–6,000 mPa·s range |
| Suspensibility Test Apparatus | CIPAC MT 15 compliant |
Test Report Dossiers
Download the Actual Laboratory Test Reports
The same bilingual controlled records our quality team closes against — structure, methods, criteria and results, with confidential fields removed. Each dossier maps to one of the seven inspection gates.
IQC — Incoming Material Reports
Active ingredient, solvent, surfactant and component verification against the approved specification.
Download IQC reports (PDF)IPQC — In-Process & First Article Reports
First article and in-process inspection records against the locked revision.
Download IPQC reports (PDF)Stability — Accelerated & Shelf-Life Records
100% batch 54 °C accelerated stability, suspensibility, and active content verification.
View QC/QA document libraryFQC — Final Product Test Reports
Final inspection against the approved sample — active content, physical properties, and specification compliance.
Download FQC reports (PDF)PSI — Packing & Pre-Shipment Reports
Kit completeness, barcode grade, carton markings and drop-safety records.
Download PSI reports (PDF)Shipment Release & Traceability Dossier
Release authorization and batch traceability mapped to spec, label and BOM.
Download release reports (PDF)Complete Quality Dossier
One pack covering the whole documentation system — QIP, gate records, traceability and NCR control.
Download documentation pack (PDF)Audit the Lab Behind Your Order
The lab operates independently from production and reports directly to management. Review the test reports, visit the inspection standards, or request a live lab walkthrough during production planning.