Zdrowie i gospodarka · 13/04/2000

FDA Announces OMB Approval for Medical Device Reporting Requirements Under FDAMA

The Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) for a collection of information related to reporting and recordkeeping requirements for medical device manufacturers, importers, and distributors, as mandated by the Food, Drug, and Cosmetic Act (FDAMA).