[1]
J. Carlos de Souza, “Evaluation of Adverse Events Recorded in FDA/USA and ANVISA/Brazil Databases for Medical Devices: Defibrillator, Infusion Pump, Physiological Monitor, Pulmonary Ventilator and Ultrasonic Scalpel”, GlobalCE, vol. 4, no. 2, pp. 5-14, Jun. 2021.