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Start Over Subjects United States ✖ Copyright Public domain ✖ Publication Year 2020 ✖

241. Considerations for defining rural places in health policies and programs

Author(s):: Mueller, Keith J., author
Coburn, Andrew F., author
Knudson, Alana, author
Lundblad, Jennifer P., author
MacKinney, A. Clinton, author
McBride, Timothy, author
Mobley, Erin, author
Ullrich, Fred, author
Barker, Abigail, author
Publication:: [Iowa City, Iowa] : Rural Policy Research Institute, May 2020
Subject(s):: Health Policy
Rural Health Services
Rural Population
Terminology as Topic
United States

242. The effects of pandemic-related legislation on output

Publication:: [Washington, DC] : Congressional Budget Office, September 2020
Subject(s):: Coronavirus Infections -- economics
Gross Domestic Product
Pandemics -- economics
Pandemics -- legislation & jurisprudence
United States

243. Who went without health insurance in 2019, and why?

Publication:: [Washington, DC] : Congressional Budget Office, September 2020
Subject(s):: Insurance Coverage -- statistics & numerical data
Medically Uninsured -- statistics & numerical data
United States

244. Policies to achieve near-universal health insurance coverage

Publication:: [Washington, DC] : Congressional Budget Office, October 2020
Subject(s):: Health Policy
Universal Health Insurance
United States

245. Use of serological tests to reduce the risk of transfusion-transmitted human T-lymphotropic virus types I and II (HTLV-I/II)

Publication:: Silver Spring, MD : Center for Biologics Evaluation and Research, February 2020
Subject(s):: Blood Transfusion -- standards
HTLV-I Antibodies -- blood
HTLV-II Antibodies -- blood
HTLV-I Infections -- transmission
HTLV-II Infections -- transmission
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

246. Peripheral vascular atherectomy devices: premarket notification [510(k)] submissions : guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, February 13, 2020
Subject(s):: Atherectomy -- instrumentation
Device Approval
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

247. Providing regulatory submissions in electronic format: certain human pharmaceutical product applications and related submissions using the eCTD specifications

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, February 2020
Subject(s):: Drug Approval
Electronic Data Processing
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

248. Recommendations for clinical laboratory improvement amendments of 1988 (CLIA) waiver applications for manufacturers of in vitro diagnostic devices: guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, February 26, 2020
Subject(s):: Clinical Laboratory Techniques -- standards
Diagnostic Errors
Reagent Kits, Diagnostic -- standards
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

249. Recommendations for dual 510(k) and CLIA waiver by application studies: guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, February 26, 2020
Subject(s):: Clinical Laboratory Techniques
Device Approval
Reagent Kits, Diagnostic
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

250. Bone anchors: premarket notification (510(k)) submissions : guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, March 3, 2020
Subject(s):: Device Approval
Suture Anchors
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

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