We work according to applicable legal standards and procedures to ensure quality in all facets. The staff of the Quality Assurance and Regulatory Affairs department are fully aware of the latest legislation and standards. They guarantee the internal implementation of the current requirements. The product information files, including Safety assessments are prepared in collaboration with independent qualified assessors. We furthermore carry out in-house microbiological research, performed by our Quality Control department

We work in accordance with the applicable requirements within the cosmetics industry, Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 11 July 2013 on cosmetic products. We also work according to the statutory Good Manufacturing Practice standard (GMP ISO 22716:2007). GMP provides guidelines for the production, inspection, storage and shipment of cosmetic products.

We are EN ISO 13485:2016 certified by which we demonstrate our ability to provide medical devices and related services that consistently meet customer and European regulatory requirements applicable to medical devices and related services.

Our company is also certified under the BRC Global Standard Consumer Goods, Issue 3, Grade A standard according to which we meet the specific requirements for a quality management system.