Regulatory Affairs

Regulatory Affairs and Documentation

Our dedicated quality team ensures the implementation of uniform standards and processes for our production sites in Germany.

Our Company is GMP (good manufacturing practice), FSSC 22000/ISO 22000 and DIN EN ISO 9001 certified. Of course, our products are fully documented. Depending on the needs of individual markets and industries as well as legal requirements, we document our Mineral Salts and products according to international and national requirements.

Our regulatory affairs department is staffed by experts in the field of documentation of our products. In addition to various standard documentations, our colleagues prepare documents and dossiers, which are necessary for the registration and submission of products at international authorities.

Documents

Pharma industry

Details of the documentation for the pharmaceutical industry can be found here.

Food industry

Allergen statement
Nutritional data sheet
GMO statement
GB statement
TSE/BSE
HACCP
Heavy metals
Foreign body
Melamine statement
Solvent residues

Cosmetic industry

Documentation of origin
Documentation of additives, artificial coloring and aromatic substances
No animal testing
CMR materials
Nanomaterials
European Cosmetics Regulation
REACH

Details of the documentation for the cosmetic industry can be found here.

Industrial applications

Details on documentation for industrial applications can be found here in the section Regulatory Support.

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