Quality is not a checkpoint. It's our culture.
From raw material to finished export pallet, every link in our chain is built around pharmaceutical-grade testing, documentation and accountability.
Documented, audited, accountable.
Quality Management System
ISO 9001:2015 aligned QMS with documented SOPs covering every production and laboratory function.
Standard Operating Procedures
Step-by-step SOPs for manufacturing, packaging, sampling, testing, calibration and deviations.
Batch Documentation
Complete batch manufacturing and packaging records with full traceability from raw material to despatch.
Three layers of quality control.
Raw Material Inspection
Every incoming material is sampled and tested against pre-approved specifications before release for production.
In-Process Quality Control
Critical parameters (pH, density, viscosity, fill weight, assay) monitored at defined checkpoints during manufacturing.
Finished Goods Testing
Physical, chemical, microbiological and stability testing of every finished batch prior to commercial release.
Traceable. Auditable. Exportable.
Every batch we manufacture is supported by a comprehensive set of documents — Batch Manufacturing Record, Batch Packaging Record, Certificate of Analysis, Material Safety Data Sheet and shipment-ready export documentation. Documents are version controlled and archived per regulatory retention norms.
- Batch Manufacturing Records (BMR)
- Batch Packaging Records (BPR)
- Certificate of Analysis (CoA) for every batch
- Material Safety Data Sheets (MSDS)
- Stability study protocols & reports
- Calibration & validation records
- Deviation, change control and CAPA logs
- Export documentation (COO, COPP, free sale certificates)