이 기사의 번역을 준비하고 있습니다. 그동안 영어 원문을 임시로 표시합니다.
비즈니스 · 2009. 6. 24.1 분 읽기
The Essentials of Medical Device Regulations: A Primer for Manufacturers and Importers; Public Seminar
로컬 자동 번역 · 원본 출처 언어
요약
The Food and Drug Administration's (FDA's) Center for Devices and Radiological Health and Office of Regulatory Affairs, in cooperation with AdvaMed's Medical Technology Learning Institute, is announcing a series of three public seminars on FDA medical device regulations. These 2-day public seminars, which are designed to address the training needs of startup and small device manufacturers and their suppliers, will include both industry and FDA perspectives and a question and answer period.
원본 출처 언어: Federal Register — Food and Drug Administration원문 발표 열기 →