The Center for Devices and Radiological Health (CDRH), the section of the Food and Drug Administration (FDA) responsible for the regulation of medical devices, has issued a request for public comments on expanding patient access to medical technologies intended for use by patients in their homes. The June 1, 2023 notice from CDRH includes a list of specific questions on which the agency is requesting feedback and can be found here….
By: Mintz
By: Mintz
