At CellArtgen Lab Pvt. Ltd., our production operations are conducted in full compliance with current Good Manufacturing Practices (cGMP) and all applicable global regulatory guidelines. Our Head of Production is a highly qualified professional with extensive experience in pharmaceutical manufacturing techniques and operations.
Every batch manufactured at our facility follows a rigorous process — from initiation to final dispatch. Batch Manufacturing Records are updated online and completed at every stage of production. All manufacturing is carried out strictly in accordance with the Master Formula Record (MFR), ensuring complete traceability and consistency in every batch.
Packaging operations begin only after formal clearance from the Quality Assurance department. Reconciliation is performed at all critical steps of manufacturing and upon completion of packaging operations — ensuring zero discrepancies and full accountability.
Our Annual Production Capacity
60M+
General Tablets
90M+
Hard Gelatin Capsules
15M+
Syrups
30M+
Dry Powder Injections
200M+
Beta-Lactam Units
Production Capacity Overview
| S. No. | Product Category | Annual Capacity |
|---|---|---|
| 1 | General Tablet Section | 60.00 Million |
| 2 | Hard Gelatin Capsule Section | 90.00 Million |
| 3 | Syrups Section | 15.00 Million |
| 4 | Dry Powder Injection Section | 30.00 Million |
| 5 | Beta-Lactam Section | 200.00 Million |
Quality Systems in Production
🔬 Quality Control System
Our Quality Control department is fully independent of the Production area. It holds complete authority to approve or reject all components, drug products, containers, closures, packaging materials, and labelling. No product is released for sale or supply until its quality has been verified and judged satisfactory through rigorous testing and documentation.
🛡️ Quality Assurance System
Our Quality Assurance department conducts comprehensive stability studies on all products to determine and assign shelf life under prescribed storage conditions. All stability study records are maintained systematically in the QA Documentation Room, ensuring complete traceability and compliance at all times.
