Quality You
Can Verify
Every batch of Vetrux CBD isolate is produced under cGMP conditions, tested by accredited third-party laboratories, and documented with full traceability from hemp biomass to finished product.
Manufacturing standards align with ICH Q7 (Active Pharmaceutical Ingredient GMP), EU GMP Annex 1 (sterile and controlled-environment manufacturing principles), and FDA 21 CFR Part 211 current Good Manufacturing Practice regulations. Industry data indicates that inadequate supplier qualification contributes to over 60% of pharmaceutical quality failures — Vetrux's 5-stage QA pipeline is designed to eliminate this risk at source. (ICH Q10 Pharmaceutical Quality System)
Certifications
Independently Verified Standards
All certifications are current, verifiable through the issuing bodies, and available for review as part of the supplier qualification process.
ISO 9001:2015
Quality management system — independently audited and certified.
GMP Certified
Good Manufacturing Practice aligned with ICH Q7 for pharmaceutical API production.
HACCP
Hazard Analysis and Critical Control Points — food safety management system.
ISO/IEC 17025
Third-party laboratory testing accreditation for all analytical results.
Learn more about evaluating supplier certifications in our supplier due diligence checklist →
Analytical Testing
Full Analytical Panel — Every Batch
No sampling shortcuts. Every production batch undergoes the complete testing panel before release, with results documented in a batch-specific Certificate of Analysis.
Cannabinoid Profile
HPLC-UV — USP reference standards
CBD ≥99.5%, THC ND, full minor cannabinoid panel
Residual Solvents
GC-MS — ICH Q3C Class I/II/III
Total residual solvents <10 PPM
Heavy Metals
ICP-MS — USP <232> / <233>
Pb, As, Cd, Hg — quantitative results per batch
Microbial Limits
USP <61> / <62> — Pharmacopeial
TAMC, TYMC, Salmonella, E. coli, S. aureus
Pesticide Residues
LC-MS/MS — EU MRL panel
400+ pesticide screen — ND for all regulated compounds
Mycotoxins
ELISA / LC-MS — EU limits
Aflatoxins B1/B2/G1/G2, Ochratoxin A — ND
Understand what each COA section means: How to read a CBD Certificate of Analysis →
Quality Process
5-Stage Quality Assurance Pipeline
Incoming Biomass QC
Every hemp biomass lot tested for cannabinoid content, moisture, pesticides, and mycotoxins before acceptance.
In-Process Controls
Potency checks at extraction, winterization, and chromatography stages. Deviations trigger CAPA investigation.
Final Product Testing
Full analytical panel on every finished batch — cannabinoid profile, residual solvents, heavy metals, microbial limits.
Third-Party Verification
Independent COA from ISO/IEC 17025-accredited laboratory before batch release. No exceptions.
Stability Monitoring
ICH Q1A-compliant stability program with testing at 0, 3, 6, 12, 18, and 24 months.
COA samples, certification copies, and audit access available to qualified B2B buyers.