DataRiver offers its expertise in the development of clinical studies on medical devices of class I, IIa, IIb and III. Following the coming into force of the new regulation on medical devices (EU) 2017/745 on 25 May 2017, clinical studies will be essential in the development and life-cycle of medical devices, for obtaining and/or maintaining the CE brand. The experience gained in this field makes DataRiver a reliable partner to turn to.
Case studies
In conformity with Article 26 of the Legislative Decree of August 5, 2022 and the Guidelines of the Italian Ministry of Health March 28, 2013 and December 20, 2017, the information in this section of the website is intended only for healthcare professionals. By selecting Continue, you declare that you are a healthcare professional, allowing you to continue to access the area dedicated to the ARIA medical device.
In conformity with Article 26 of the Legislative Decree of August 5, 2022 and the Guidelines of the Italian Ministry of Health March 28, 2013 and December 20, 2017, the information in this section of the website is intended only for healthcare professionals. By selecting Continue, you declare that you are a healthcare professional, allowing you to continue to access the area dedicated to the ARIA medical device.
