Regulatory skeleton of medical devices in the european union Kalva Soundarya Reddy1, Kalva Sahitya Reddy2, Haripriya3 111430 Hayloft ln, Glen Allen, Virginia, USA, 23060: +1 (804) 874-5928 2Kaseya Software Company, Ground Floor, Tower B, Prestige Shantiniketan, Mahadevpura, Whitefield 350832, Sevilla Circle, Novi, MI, 48374, USA Online Published on 29 March, 2024. Abstract ‘Medical device’ means any instrument, apparatus, implement, machine, appliance, implant, reagent for in vitro use, software, material or other similar or related article, intended by the manufacturer to be used, alone or in combination, for human beings, for one or more of the specific medical purpose(s). Medical devices make an essential contribution to healthcare in the Europe for the benefit of European citizens. These products must undergo a conformity assessment to demonstrate that they meet legal requirements to ensure they are safe and perform as intended. The European Medicines Agency (EMA) is responsible for the scientific evaluation of a product through centralized marketing authorisation applications (MAA). In order to commercialize medical devices in the European Union, a (European Conformity) CE Mark certificate is needed. Top Keywords Medical Device, European Commission, MDR, Centralized Procedure, European Medicines Agency. Top |