Ensuring the Conformity of the medical device to the Medical Device Regulation and Quality Management System, Ensure that EU declaration of conformity and technical documentation are drawn up and kept up to-date, Communicating with the Regulatory Authorities as and when required, Reporting Obligations (Vigilance, trend reporting, analysis of serious incidents and field safety corrective actions, analysis of vigilance data), Ensure Post-Market Surveillance Compliance.
Masqué
Cartographie de Nectar Laboratories Private Limited