Recently an announcement of a Public Workshop was posted on Federal Register (FR). This workshop, “Accessible Medical Device Labeling in a Standard Content and Format,” is to investigate the growing need for medical devices to be labeled in a clear and concise manner. Currently, there is a lack of direct regulation that defines a standard for medical device labeling. FDA hopes this workshop will begin the process of establishing a standard.
Topics: Patients, Federal Register, Device Labeling, FDA