Documentation is central to pharmaceutical manufacturing, and at Virupaksha Organics Ltd, it forms the core of its cGMP (current Good Manufacturing Practice) compliance. Every activity—from raw material procurement to batch release—is meticulously recorded and traceable.
The company employs a robust digital documentation system that supports audit-readiness and eliminates risks associated with manual errors. This ensures all processes are transparent, reproducible, and verifiable in real-time.
Well-maintained records help in faster regulatory approvals and also foster accountability across departments. Virupaksha’s documentation culture reinforces its commitment to manufacturing excellence and product integrity in the global pharmaceutical market.
