We provide a full range of services for medical devices.
CE plus is an international affiliate of Montrose R+, specializing in regulatory strategy and implementation for medical devices and in vitro diagnostics. The core competency of CEplus lies in CE marking for European markets, customized quality management systems, and any other activities that help clients realize market success.
CE plus’ relationship with regulanet® allows them to access resources and manage complex international projects.
CE plus uses interdisciplinary teams to develop project-specific solutions tailored to clients’ needs, helping them maximize market asset value.
For more information, visit us at: www.ceplus.eu
