Salin Consulting Your regulatory translator for the practice and the innovation

We make sure that your products will be compliant with the following directives respectively for In Vitro Diagnostic (IVD) and general Medical devices but we are here with you from a manufacturer perspective to support you in workshops In House, External and Internal Auditor Services, Preparation for Audit with competent authorities, Risk Management system and files verification, Counsel and analysis on In Vitro Diagnostic for medical device manufacturers. Complementary we offer content management on social media. Marie Salin is an experienced Managing Director with a demonstrated history of working in the medical device industry. Skilled in Medical Devices, Sales Management, Biotechnology, Management, product development and registration. Expert of the european market and medical regulations of the territory, Marie is fluent in German, French and English.