Integration of FDA and NIOSH Processes Used to Evaluate Respiratory Protective Devices for Health Care Workers (Paperback)

Idioma: inglés

Editorial: National Academies Press, Washington, 2017

0309451272 / 9780309451277

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Paperback. Both the Food and Drug Administration (FDA) and the National Institute for Occupational Safety and Health (NIOSH) have responsibilities for evaluating and regulating respiratory protective devices (a /respiratorsa ) for health care workers. Respirators protect the user from respiratory hazards by either removing contaminants from the air (air-purifying respirators) or by supplying clean air from another source (air-supplying respirators). Respirators that are used in workplaces in the United States must be approved by NIOSH and meet standards and test results specified by regulation. Respirators used by health care workers are air-purifying respirators that generally fall into three types: (1) disposable particulate filtering facepiece respirators (also termed N95s); (2) elastomeric respirators, also known as reusable respirators because they use a replaceable filter; or (3) powered air-purifying air respirators.To provide input to NIOSH and FDA and to discuss potential next steps to integrate the two agenciesa (TM) processes to certify and approve N95 respirators for use in health care settings, a workshop was held by the National Academies of Sciences, Engineering, and Medicine in August 2016. The workshop was focused on exploring the strengths and limitations of several current test methods for N95 respirators as well as identifying ongoing research and research needs. This publication summarizes the presentations and discussions from the workshop. Respirators that are used in workplaces in the United States must be approved by NIOSH and meet standards and test results specified by regulation.Respirators used by health care workers are air-purifying respirators that generally fall into three types: (1) disposable particulate filtering facepiece respirators (also termed N95s); Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.…

N° de ref. del artículo 9780309451277

Título
Integration of FDA and NIOSH Processes Used to Evaluate Respiratory Protective Devices for Health Care Workers (Paperback)
Autor
Health and Medicine Division
Editorial
National Academies Press, Washington
Año de publicación
2017
Estado
new
Encuadernación
Paperback
Idioma
inglés
ISBN 10
0309451272
ISBN 13
9780309451277

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The Nile Group Pty Ltd

42 Apex Drive
Truganina, VIC Australia 3029