Цей переклад готується. Тимчасово ми показуємо оригінальну версію англійською мовою.
Бізнес · 08.02.20111 хв читання
Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers
Локальний автоматичний переклад · Оригінальна мова джерела
Короткий зміст
The Food and Drug Administration (FDA) is announcing that a collection of information entitled "Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers" has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Оригінальна мова джерела: Federal Register — Health and Human ServicesВідкрити оригінальне повідомлення →