Quality is not a check at the end of the line. It is a set of documented decisions taken at every point before it.
Certificates are available to partners on request. Our documentation travels with the product.
Our facility is operated and audited against the WHO's Good Manufacturing Practice guidelines, covering premises, personnel, process control and batch release — the reference standard for pharmaceutical and nutraceutical manufacturing worldwide.
Compliance with India's food safety framework across ingredient permissibility, label accuracy, additive limits and manufacturing hygiene — the mandatory basis for any consumer health product sold in India.
Our quality management system is certified to ISO 9001, which governs process consistency, documentation control and continuous improvement across the whole operation, not only the production floor.
A finished product carries the accumulated decisions of everyone who touched it. So we test at the points where a problem can still be caught cheaply, rather than discovering it at release when the only option left is to destroy the batch.
By the time a unit leaves the facility it has been checked five separate times, by five separate criteria, and the record of each check stays with its lot number permanently.
Incoming materials tested for identity, purity, potency and contamination before acceptance. Only vendors who have passed qualification and can document provenance are used.
Blend uniformity, weight variation, hardness and dissolution monitored at defined intervals through the run, with microbial controls throughout.
HPLC assay for active content, dissolution testing, microbial limits, heavy metal screening, and full specification compliance before anything is packed.
Pack integrity verification, plus accelerated and real-time stability studies that establish shelf life under the storage conditions printed on the label.
Formal review and sign-off by qualified personnel, with complete batch records, certificate of analysis and regulatory documentation, before a single unit leaves the site.
Controlled environment production with defined air classifications and contamination prevention protocols.
Every process governed by a written Standard Operating Procedure, with deviations recorded and investigated.
Trained quality professionals and regulatory specialists accountable for compliance at each operational level.
Complete records from raw material lot to finished unit, traceable in both directions for every batch produced.
Every ingredient comes from a qualified supplier with full documentation. We test what we say we use, and we use what we say we test.
What the label declares is what the product contains, verified by analytical testing for active content within approved tolerance limits.
Microbial testing, heavy metal screening and contaminant analysis are performed on every batch, without exception and without shortcuts.
Certificates of analysis, stability data, facility certifications and regulatory documentation — available to partners under NDA.