ObjectiveThis SOP defines the complete risk management process for medical devices and medicinal products of Divisions Hospital Care and Out Patient Market (OPM) during development as well as commercial phase,- in order to avoid endangering a patient, a user, a third party or the environment when using medical devices or medicinal products,- in order to document a reproducible identification and estimation of the risks and the measures taken to control these risks.The risk management process includes risk analysis, risk evaluation and the risk control across the whole life-cycle of medical devices and medicinal products. It defines the process steps and sets out the responsibilities and times of application.
đang được dịch, vui lòng đợi..
