Sodium Chondroitin Sulfate produced with
traceability, documentation and safety in mind.
Our Sodium Chondroitin Sulfate products are of the best possible quality and comply with several international standards for pharmaceuticals i.e. the European Pharmacopoeia, the Japanese Pharmaceutical Codex, the US Pharmacopoeia and the British Pharmacopoeia.
Our manufacturing facility is in compliance with the rules governing medicinal products in the European Union laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively.
We hold a Manufacturer’s/Importer’s authorization regarding Human Medicinal Products issued by the Danish Health and Medicines Authority.
We also hold Certificate of EU-GMP, JP-GMP and cGMP compliance on manufacturing of Sodium Chondroitin Sulfate according to the European Pharmacopoeia and the Japanese Pharmacopoeia.
Furthermore, we are registered at the Danish Health and Medicines Authority as an Active Pharmaceutical Ingredients manufacturer.
Would you like to know more about our GMP Compliance or certifications, feel free to contact us at firstname.lastname@example.org.