Yannan Xu

Clinical Affairs: - Preparation and review of clinical evaluation for medical devices of all risk classes according to MEDDEV 2.7/1 Rev.4, MDD, Medical Device Regulation (EU) 2017/745 and CFDA Announcement 2015 No.14. Regulatory Affairs: - Support for medical device registration in China according to the Regulations on the Supervision and Administration of Medical Devices No. 739.

- Erstellung von Klinischen Bewertung nach MEDDEV 2.7/1, Verordnung (EU) 2017/745 und CFDA/NMPA (China Food and Drug Administration/National Medical Products Administration) über Medizinprodukte - Systematische Literatursuche in einschlägigen Datenbanken (EMBASE, PubMed, CNKI etc.) - Auswertung Klinischer Erfahrungsdaten (Post Market Surveillance)