Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers :: proceedings of a workshop /
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 ("respirators") for health care workers. Respirators protect the user from respiratory hazard...
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| Format: | Elektronisch Tagungsbericht E-Book |
| Sprache: | English |
| Veröffentlicht: |
Washington, DC :
The National Academies Press,
[2017]
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| Schlagworte: | |
| Online-Zugang: | DE-862 DE-863 |
| Zusammenfassung: | 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 ("respirators") 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 agencies' 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. |
| Beschreibung: | 1 online resource (1 PDF file (xi, 63 pages)) |
| Bibliographie: | Includes bibliographical references. |
| ISBN: | 9780309451277 0309451272 0309451280 9780309451284 |
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| 520 | 3 | |a 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 ("respirators") 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 agencies' 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. | |
| 536 | |a This activity was supported by Award #10002969 between the National Academy of Sciences and the Department of Health and Human Services' Centers for Disease Control and Prevention. Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project. | ||
| 588 | 0 | |a Online resource; title from PDF title page (viewed May 26, 2017). | |
| 505 | 0 | |a Introduction -- Perspectives from users, manufacturers, and distributors -- Exploring the state of the science and potential priorities for research and standards development -- Options for post-market surveillance -- Potential next steps and priorities -- References -- Appendix A: Workshop agenda -- Appendix B: Workshop participants. | |
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| 651 | 2 | |a United States |0 https://id.nlm.nih.gov/mesh/D014481 | |
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| 776 | 0 | 8 | |i Print version: |a Liverman, Catharyn T. |t Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers. Proceedings of a Workshop. |d Washington, District of Columbia : National Academies Press, ©2017 |h xi, 63 pages |z 9780309451277 |
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| contents | Introduction -- Perspectives from users, manufacturers, and distributors -- Exploring the state of the science and potential priorities for research and standards development -- Options for post-market surveillance -- Potential next steps and priorities -- References -- Appendix A: Workshop agenda -- Appendix B: Workshop participants. |
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| illustrated | Not Illustrated |
| indexdate | 2025-03-18T14:23:21Z |
| institution | BVB |
| institution_GND | http://id.loc.gov/authorities/names/n2016187520 http://id.loc.gov/authorities/names/no2017035121 |
| isbn | 9780309451277 0309451272 0309451280 9780309451284 |
| language | English |
| oclc_num | 976013359 |
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| physical | 1 online resource (1 PDF file (xi, 63 pages)) |
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| publishDate | 2017 |
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| publisher | The National Academies Press, |
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| spelling | Liverman, Catharyn T., rapporteur. http://id.loc.gov/authorities/names/n95019366 Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / Catharyn T. Liverman and Joe Alper, rapporteurs ; Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. Washington, DC : The National Academies Press, [2017] 1 online resource (1 PDF file (xi, 63 pages)) text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references. 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 ("respirators") 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 agencies' 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. This activity was supported by Award #10002969 between the National Academy of Sciences and the Department of Health and Human Services' Centers for Disease Control and Prevention. Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project. Online resource; title from PDF title page (viewed May 26, 2017). Introduction -- Perspectives from users, manufacturers, and distributors -- Exploring the state of the science and potential priorities for research and standards development -- Options for post-market surveillance -- Potential next steps and priorities -- References -- Appendix A: Workshop agenda -- Appendix B: Workshop participants. United States. Food and Drug Administration. http://id.loc.gov/authorities/names/n80126147 National Institute for Occupational Safety and Health. http://id.loc.gov/authorities/names/n79063156 United States. Food and Drug Administration. National Institute for Occupational Safety and Health. National Institute for Occupational Safety and Health fast United States. Food and Drug Administration fast Breathing apparatus United States Congresses. Medical personnel. http://id.loc.gov/authorities/subjects/sh85082982 Respiratory Protective Devices standards https://id.nlm.nih.gov/mesh/D012134Q000592 Equipment Safety standards https://id.nlm.nih.gov/mesh/D004869Q000592 Government Agencies https://id.nlm.nih.gov/mesh/D006077 Government Regulation https://id.nlm.nih.gov/mesh/D033161 Health Personnel https://id.nlm.nih.gov/mesh/D006282 Occupational Exposure prevention & control https://id.nlm.nih.gov/mesh/D016273Q000517 United States https://id.nlm.nih.gov/mesh/D014481 Respirateurs États-Unis Congrès. Personnel médical. Medical personnel fast Breathing apparatus fast United States fast https://id.oclc.org/worldcat/entity/E39PBJtxgQXMWqmjMjjwXRHgrq Congress https://id.nlm.nih.gov/mesh/D016423 proceedings (reports) aat Conference papers and proceedings fast Conference papers and proceedings. lcgft http://id.loc.gov/authorities/genreForms/gf2014026068 Actes de congrès. rvmgf Alper, Joe, author. National Academies of Sciences, Engineering, and Medicine (U.S.). Board on Health Sciences Policy, issuing body. http://id.loc.gov/authorities/names/n2016187520 Integration of FDA and NIOSH Processes Used to Evaluate Respiratory Protective Devices for Health Care Workers (Workshop) (2016 : Washington, D.C.) http://id.loc.gov/authorities/names/no2017035121 Print version: Liverman, Catharyn T. Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers. Proceedings of a Workshop. Washington, District of Columbia : National Academies Press, ©2017 xi, 63 pages 9780309451277 |
| spellingShingle | Alper, Joe Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / Introduction -- Perspectives from users, manufacturers, and distributors -- Exploring the state of the science and potential priorities for research and standards development -- Options for post-market surveillance -- Potential next steps and priorities -- References -- Appendix A: Workshop agenda -- Appendix B: Workshop participants. United States. Food and Drug Administration. http://id.loc.gov/authorities/names/n80126147 National Institute for Occupational Safety and Health. http://id.loc.gov/authorities/names/n79063156 United States. Food and Drug Administration. National Institute for Occupational Safety and Health. National Institute for Occupational Safety and Health fast United States. Food and Drug Administration fast Breathing apparatus United States Congresses. Medical personnel. http://id.loc.gov/authorities/subjects/sh85082982 Respiratory Protective Devices standards https://id.nlm.nih.gov/mesh/D012134Q000592 Equipment Safety standards https://id.nlm.nih.gov/mesh/D004869Q000592 Government Agencies https://id.nlm.nih.gov/mesh/D006077 Government Regulation https://id.nlm.nih.gov/mesh/D033161 Health Personnel https://id.nlm.nih.gov/mesh/D006282 Occupational Exposure prevention & control https://id.nlm.nih.gov/mesh/D016273Q000517 Respirateurs États-Unis Congrès. Personnel médical. Medical personnel fast Breathing apparatus fast |
| subject_GND | http://id.loc.gov/authorities/names/n80126147 http://id.loc.gov/authorities/names/n79063156 http://id.loc.gov/authorities/subjects/sh85082982 https://id.nlm.nih.gov/mesh/D012134Q000592 https://id.nlm.nih.gov/mesh/D004869Q000592 https://id.nlm.nih.gov/mesh/D006077 https://id.nlm.nih.gov/mesh/D033161 https://id.nlm.nih.gov/mesh/D006282 https://id.nlm.nih.gov/mesh/D016273Q000517 https://id.nlm.nih.gov/mesh/D014481 https://id.nlm.nih.gov/mesh/D016423 http://id.loc.gov/authorities/genreForms/gf2014026068 |
| title | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / |
| title_auth | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / |
| title_exact_search | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / |
| title_full | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / Catharyn T. Liverman and Joe Alper, rapporteurs ; Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. |
| title_fullStr | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / Catharyn T. Liverman and Joe Alper, rapporteurs ; Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. |
| title_full_unstemmed | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : proceedings of a workshop / Catharyn T. Liverman and Joe Alper, rapporteurs ; Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. |
| title_short | Integration of FDA and NIOSH processes used to evaluate respiratory protective devices for health care workers : |
| title_sort | integration of fda and niosh processes used to evaluate respiratory protective devices for health care workers proceedings of a workshop |
| title_sub | proceedings of a workshop / |
| topic | United States. Food and Drug Administration. http://id.loc.gov/authorities/names/n80126147 National Institute for Occupational Safety and Health. http://id.loc.gov/authorities/names/n79063156 United States. Food and Drug Administration. National Institute for Occupational Safety and Health. National Institute for Occupational Safety and Health fast United States. Food and Drug Administration fast Breathing apparatus United States Congresses. Medical personnel. http://id.loc.gov/authorities/subjects/sh85082982 Respiratory Protective Devices standards https://id.nlm.nih.gov/mesh/D012134Q000592 Equipment Safety standards https://id.nlm.nih.gov/mesh/D004869Q000592 Government Agencies https://id.nlm.nih.gov/mesh/D006077 Government Regulation https://id.nlm.nih.gov/mesh/D033161 Health Personnel https://id.nlm.nih.gov/mesh/D006282 Occupational Exposure prevention & control https://id.nlm.nih.gov/mesh/D016273Q000517 Respirateurs États-Unis Congrès. Personnel médical. Medical personnel fast Breathing apparatus fast |
| topic_facet | United States. Food and Drug Administration. National Institute for Occupational Safety and Health. National Institute for Occupational Safety and Health United States. Food and Drug Administration Breathing apparatus United States Congresses. Medical personnel. Respiratory Protective Devices standards Equipment Safety standards Government Agencies Government Regulation Health Personnel Occupational Exposure prevention & control United States Respirateurs États-Unis Congrès. Personnel médical. Medical personnel Breathing apparatus Congress proceedings (reports) Conference papers and proceedings Conference papers and proceedings. Actes de congrès. |
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