Deluxe Dossier is a collective of Regulatory Affairs Professionals with a proven ability to use and apply technical standards, principles, theories, concepts, and techniques. We are very dedicated and can multi-task and meet or exceed deadlines. We are experienced in medical device global regulatory filings (Including U.S. and EU) for Class I, Class II, Class IIa & Class III medical devices. We provide Regulatory Affairs Consulting services as well as Regulatory Affairs training. Deluxe Dossier