Request for information and public comment

Not later than 2 years after the date of enactment of this Act, the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall post a request for information including a public docket in the Federal Register and on a publicly accessible website of the Department of Health and Human Services enabling stakeholders to submit comments on how to continue to optimize the format, accessibility, and usability of electronic labeling of devices other than prescription devices intended for use in health care facilities or by a health care professional and in vitro diagnostic devices intended for use by health care professionals or in blood establishments.