European Authorized Representative & CE Marking
Obelis European Authorized Representative Center (O.E.A.R.C.) provides CE Marking regulatory compliance consulting to manufacturers worldwide, in accordance with European Directives such as MDD 93/42/EEC, IVD 98/89/EC , and Low Voltage Devices 73/23/EEC . Our high quality compliance solutions, proven by our ISO 9002 certification, include Commercial, Regulatory, Administrative, and Market Development Services through our Brussels, Belgium headquarters. Our worldwide regulatory solutions are provided through our global and professional One Link One Solution"! Network.

Qserve Consultancy provides coordinated European and American regulatory and quality strategic planning, guidance and implementation from design and development through to market launch, including all regulatory documentation and submissions, to medical device companies worldwide. Our clients include manufacturers of high risk products such as pacemakers and catheters.