Quality Program
Certainty,
documented.
A batch leaves our docks only after three independent analyses agree, two analysts sign, and every document a regulator could ask for is already in the box.
01 — Documentation
The COA that
survives audits.
A certificate of analysis should be evidence, not marketing. Ours carries the instrument ID, the analyst's signature, and the raw HPLC trace — so your QA team can verify rather than trust.
Every shipment includes: COA with method references, MSDS, allergen declaration, IFRA statement where relevant, and regulatory dossier (EU/US) on request.
QC-07
Rawess
02 — Analysis
Three analyses.
Two signatures. One standard.
Every batch, regardless of value or volume, passes the same gate sequence before release.
Retention time and spectral fingerprint matched against in-house reference standards, not supplier claims.
Quantitative assay with full impurity profile; heavy metals by ICP-MS down to sub-ppm sensitivity.
Aerobic count, yeast & mold, and objectionable organisms screened per pharmacopoeial limits.
Analyst and reviewer reconcile independently. No single person can release a batch. Ever.
03 — Certification
Paper walls,
built to hold.
Certifications are the floor, not the ceiling. Each is audited annually by an accredited third party.
Certificate registry numbers and audit summaries available under NDA. Request documentation →
Audit us first.
Formulators who switch to Rawess usually start by testing our claims. We encourage it — send the sample to your own lab.