Driven by Innovation, Built for Excellence
One integrated manufacturing unit — fully automated, sealed, and built to deliver pharmaceutical-grade psyllium at scale.
3,500 MT
Annual Processing Capacity
1 Lakh sq.ft
Total Facility Size
50+
Employees
1 Unit
Integrated Manufacturing
Processing Technology
Precision Engineering Behind the Machines
Equipped with a fully automated and sealed processing system, our facility ensures uninterrupted production flow. Pneumatic conveying technology minimizes human intervention, delivering superior hygiene, precision, and consistent product quality.
Self-Automated Closed Processing Unit
From raw material to finished psyllium product, our fully sealed, end-to-end closed process delivers uncompromising purity, zero manual intervention, and pharmaceutical-grade hygiene.
Automated Material Pre-Cleaning System
This initial cleaning stage enhances product purity, protects downstream equipment, and contributes to consistent product quality across every production run.
Automated Color & Defect Sorting System
Our Advanced Optical Sorting System utilizes high-resolution cameras and intelligent optical technology to detect and remove discolored, damaged, and foreign materials with exceptional accuracy.
Precision Grinding & Milling Machine
Our Advanced Grinding & Milling System employs state-of-the-art processing technology to produce finely milled psyllium with exceptional consistency and controlled particle size distribution.
Moisture Management & Drying Solutions
Advanced moisture management and drying systems for precise humidity control, efficient drying, and consistent performance — optimizing product quality across all grades.
Quality Systems
Quality Assurance & Control
Excellence in Every Detail
Every product is validated through our advanced in-house QA/QC laboratory — pre-production, in-process, and final inspections complemented by comprehensive physical, chemical, and microbiological testing, with independent third-party verification.
Advanced Chemical Analysis Laboratory
Compositional analysis ensuring purity, residue profiling, and specification verification in full compliance with USP, EP, and internationally recognized pharmacopoeial standards for every batch.
Physical Testing
Evaluation of particle size, swelling factor, moisture content, and bulk density — rigorously verified at every stage of production across all product grades and specifications.
Microbiological Quality Assurance
Total plate count, pathogen screening, and microbial load analysis — with independent third-party verification for all export batches and complete traceability documentation.
Stage 01
Pre-Production Inspection
Every incoming raw material undergoes rigorous quality validation — purity assessment, moisture analysis, and microbiological evaluation — all documented before processing begins.
Stage 02
In-Process Quality Check
Continuous monitoring ensures particle size, colour consistency, and critical product specifications are verified in real time throughout every stage of production.
Stage 03
Final Product Quality Check
Every finished batch is accompanied by a detailed COA, independent third-party audit reports, and complete shipment documentation for full regulatory compliance.
Schedule a Facility Visit
We welcome buyers and partners to see our processing standards first-hand.