Cosmetic development in accordance with medical guidelines.
The SQOOM active gels have been developed in accordance with the requirements of the EU Cosmetics Directive and are documented with efficacy studies. The development is based on scientific research cooperation with recognised experts and universities from all over Germany and the wider European region. The team of developers establishes its core competency in pharmaceutical as well as cosmetic formulations and production proceeds in accordance with GMP principles.
The SQOOM device has been developed in accordance with medical guidelines and certified under the Medical Devices Directive 93/42 EEC. This is the most important key regulatory instrument (European Council Directive of 14.06.1993) ensuring the safety of medical products in Europe. Registration of the ISO 9001/2000 standard represents a comprehensive quality management standard. A similary meaning for the SQOOM-device has the valid licensure "c-UL-US listed". (Underwriters Laboratory). Systems, that have this approval, are documenting that the international rules and standards correspond e.g. in the electronic switching systems, etc.. U.S. Listed signifies the approval of the product on the American and Canadian markets, which are among the strictest in the world markets. Additional important test marks or certifications of the SQOOM device:
Safety Mark Acquired, FCC Certification Mark Acquired, CE and CCC.