Бізнес · 08.03.19991 хв читання
Agency Information Collection Activities; Announcement of OMB Approval; Medical Devices: Third-Party Review Program Under the U.S./EC MRA
Локальний автоматичний переклад · Оригінальна мова джерела
Короткий зміст
The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Medical Devices: Third-Party Review Program Under the U.S./EC MRA'' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.