Quality is not a department at Pristine — it is the operating system of the plant.
Every raw material entering our facility is quarantined and tested against approved specifications before release to production. In-process checks track moisture, particle size and bulk density at defined stages, and no finished batch is released without complete compendial testing and QA sign-off.
| Laboratory Capability | Purpose |
|---|---|
| Particle size analysis | PSD conformity to grade specification |
| Moisture / LOD | Loss on drying per compendia |
| Bulk & tapped density | Flow and compressibility assurance |
| pH & conductivity | Chemical purity verification |
| Viscosity testing | CMC and co-processed grade release |
| Microbial limit testing | TAMC, TYMC and specified pathogens |
Our pharmacopoeial products are manufactured and tested to conform with Indian, British, European and US pharmacopoeia monographs. Certifications and regulatory filings are being progressively expanded — contact us for our current certificate pack.
*Update this strip with your actual current certifications before go-live.
COA, TDS, MSDS and regulatory support documents available on request.