Quality & compliance

Every batch is testable, traceable and documented

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Certifications

The standards we work to

Our facilities and sourcing partners hold the certifications expected of a pharmaceutical and cosmetic supplier in India.

GMPGood Manufacturing Practice
ISO 9001Quality management
ISO 13485Medical devices
CDSCODrug licence compliance
WHO-GMPExport-grade standard
Our process

Four checkpoints between raw material and dispatch

Incoming materials

Every raw material and packaging lot is sampled and verified against specification before it enters the floor.

In-process checks

Weight, blend uniformity and fill volume are monitored at set intervals through the production run.

Finished goods

Assay, dissolution and microbial testing are completed before a batch is released for packing.

Stability & release

Retained samples are held on stability, and a certificate of analysis ships with the batch.

Traceability

Answer an audit in minutes

Batch numbers tie back to raw material lots, operator records and QC results. If a question is ever raised about a product on a shelf, we can reconstruct its full history.

  • Batch-level records retained for the full shelf life plus one year
  • Certificate of analysis available on request for any dispatched lot
  • Documented recall procedure, rehearsed annually
  • Cold-chain handling for products that require it
Haibo quality officer answering an audit with batch records, COA, SOPs and traceability files
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