Medical Equipment Reporting (MDR): how to tell about problems with medical equipment > 자유게시판

The user agency is not obligated to talk a malfunction of tablet or a https://www.garthcharityprojects.org/forum/general-discussions/medical-reference-articles, but is able to voluntarily notify the FDA similar problems with the product using the FDA's 3500 voluntary medwatch form within the framework of program The FDA on safety awareness and reporting of adverse events.