Chondroitin Sulfate Sodium — Pharmacopoeia Grades
Chondroitin sulfate sodium manufactured and tested to compliance with the United States Pharmacopoeia (USP), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP), and Chinese Pharmacopoeia (CP) monographs. HS Biopharma states it was among the first manufacturers to bring sulfate and chloride residuals within USP limits, enabling multi-market pharmaceutical and nutraceutical registration from a single material.
CAS Number
9007-28-7
Physical Form
Fine white to off-white powder
Typical Assay
Conforms to USP / EP / JP / CP monograph limits
Origins
Bovine / Porcine typical for pharmacopoeia submissions
Purpose and Key Benefits
Regulatory-grade documentation for multi-region product registration. Same joint-health functional profile as food-grade chondroitin, with tighter impurity and residual-solvent control.
Applications
OTC joint supplements in regulated markets, pharmaceutical formulations, multi-region product lines
Certifications
NSF-GMP Registered
NSF/ANSI 173 Section 8 · FSMA and 21 CFR Part 111/117 compliant.
NSF/ANSI 173 Sec 8
ISO 9001:2015
Quality management system.
:2015 — valid to Oct 11, 2027
ISO 22000:2018
Food safety management system.
:2018 Food Safety — valid to Oct 11, 2027
ISO 14001:2015
Environmental management system.
:2015 Environmental — valid to Nov 4, 2027
ISO 45001:2018
Occupational health and safety management system.
:2018 OH&S — valid to Nov 4, 2027
FAMI-QS Certified
Specialty feed-ingredient GMP Category K.
feed-chain certification Cat K, Registration FAM-1963; renewal in process