Sodium Chondroitin Sulfate produced with
traceability, documentation and safety in mind.
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 hold certificate of GMP the on manufacturing of Sodium Chondroitin Sulfate according to the European Pharmacopoeia and the US 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 email@example.com.