Корично изображение Електронна книга

Public health effectiveness of the FDA 510(k) clearance process : measuring postmarket performance and other select topics : workshop report /

"The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act requires a manufacturer of medical devices to notify FDA of its intent to market a medical dev...

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Автор-организации: Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process.
Други автори: Wizemann, Theresa M.
Формат: Електронна книга
Език: English
Публикувано: Washington, D.C. : National Academies Press, ℗♭2011.
Предмети:
United States. > Food and Drug Administration > Congresses.
United States. > Food and Drug Administration.
Public health > Equipment and supplies > Standards > United States > Congresses.
Public health > United States > Congresses.
Device Approval.
Equipment Safety.
HEALTH & FITNESS > Safety.
United States.
Congresses.
Electronic books.
Electronic resource.
Онлайн достъп: http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=372504
Подобни документи: Print version:: Public health effectiveness of FDA 510(k) clearance process.
Онлайн достъп от Библиотека ”Паница” на Американския университет в България:

http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=372504
Провери в Paniza Library, AUBG Сигнатура: RA399.A3 P82 2011eb

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