Studio Ambiente Srl is the ideal partner for specific regulatory consultancy, for your laboratory analyses, as well as for clean room analyses and for your product and process validations. The experience gained over the years with several international customers, the professionalism, the specific skills and the internal organization allow us to assist you at 360 degrees, identifying the best regulatory and analytical strategies and to support you in the marketing of your Medical Device in the European Market, through obtaining the CE Mark in accordance with Directive 93/42/EEC and the new EU Regulation 2017/745.