Search

1661. Underwriting in the non-group health insurance market: the fundamentals

Publication:

Washington, D.C. : George Washington University, [2009]

Subject(s):

Health Care Reform
Insurance Selection Bias
Insurance, Health
Private Sector
United States

1662. Unique Device Identification System: form and content of the unique device identifier (UDI) : guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, July 7, 2021

Subject(s):

Equipment and Supplies
Product Labeling
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1663. Unique device identification: Policy regarding compliance dates for class I and unclassified devices, direct marking, and Global Unique Device Identification Database requirements for certain devices : guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, July 25, 2022

Subject(s):

Databases as Topic
Equipment and Supplies
Government Regulation
Product Labeling
United States
United States. Food and Drug Administration

1664. Unique device identification: convenience kits : guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, April 26, 2019

Subject(s):

Equipment and Supplies -- standards
Product Labeling -- standards
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1665. Unique device identification: direct marking of devices : guidance for Industry and Food and Drug administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, November 17, 2017

Subject(s):

Equipment and Supplies -- standards
Equipment Reuse -- standards
Product Labeling -- standards
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1666. Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Biologics Evaluation and Research, January 16, 2018

Subject(s):

Equipment and Supplies -- classification
Product Labeling -- standards
Product Packaging -- standards
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1667. Unique device identification: policy regarding compliance dates for class I and unclassified devices and certain devices requiring direct marking : immediately in effect guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, July 1, 2020

Subject(s):

Equipment and Supplies -- standards
Medical Device Legislation
Product Labeling
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1668. Unwanted sexual behavior: improved guidance, access to care, and training needed to better address victims’ behavioral health needs : report to congressional requesters

Publication:

Washington, DC : United States Government Accountability Office, August 2023

Subject(s):

Government Regulation
Legislation, Medical
Military Health -- legislation & jurisprudence
Sex Offenses -- prevention & control
Sexual Harassment -- prevention & control
United States
United States. Department of Defense
United States. Department of Veterans Affairs

1669. Unwinding the Medicaid continuous enrollment provision: projected enrollment effects and policy approaches

Publication:

Washington, D.C. : Office of the Assistant Secretary for Planning and Evaluation, Office of Health Policy, August 19, 2022

Subject(s):

Eligibility Determination -- statistics & numerical data
Health Policy
Insurance Coverage -- statistics & numerical data
Medicaid -- statistics & numerical data
COVID-19 -- economics
United States

1670. Updated Medicare FFS telehealth trends by beneficiary characteristics, visit specialty, and state, 2019-2021

Author(s):

Samson, Lok Wong, author
Couture, Sara J., author
Creedon, Tim B., author
Jacobus-Kantor, Laura, author
Sheingold, Steven, author

Publication:

Washington, D.C. : Assistant Secretary for Planning and Evaluation, Office of Health Policy, July 20, 2023

Subject(s):

Medicare -- statistics & numerical data
Medicare -- trends
State Government
Telemedicine -- statistics & numerical data
Telemedicine -- trends
United States

1671. Updated national survey trends in telehealth utilization and modality (2021-2022)

Author(s):

Lee, Euny C., author
Grigorescu, Violanda, author
Enogieru, Idia, author
Smith, Scott R., author
Samson, Lok Wong, author
Conmy, Ann B., author
De Lew, Nancy, author

Publication:

Washington, D.C. : Office of the Assistant Secretary for Planning and Evaluation, Office of Health Policy, April 19, 2023

Subject(s):

Facilities and Services Utilization -- statistics & numerical data
Telemedicine -- statistics & numerical data
Telemedicine -- trends
Videoconferencing -- statistics & numerical data
Videoconferencing -- trends
United States

1672. An updated policy roadmap: caring for those with complex needs

Publication:

Washington, D.C. : Bipartisan Policy Center, March 2022

Subject(s):

Health Policy
Long-Term Care
Multiple Chronic Conditions -- therapy
United States

1673. Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process": guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, September 8, 2023

Subject(s):

Biological evaluation of medical devices
Device Approval
Equipment and Supplies -- adverse effects
Government Regulation
Guidelines as Topic
United States

1674. Use of International Standard ISO 10993-1: "Biological evaluation of medical devices - part 1 : evaluation and testing within a risk management process" : guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, September 4, 2020

Subject(s):

Device Approval
Equipment Failure
Equipment Safety
Equipment and Supplies -- standards
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1675. Use of certified health IT and methods to enable interoperability by U.S. non-federal acute care hospitals: 2019

Author(s):

Johnson, Christian, MPH (based on t.p. from bib 9918317680206676), author
Pylypchuk, Yuriy, author

Publication:

Washington, DC : U.S. Department of Health and Human Services, Office of the National Coordinator for Health Information Technology, February 2021

Subject(s):

Electronic Health Records
Health Information Interoperability -- trends
Hospitals
Information Dissemination
Health Information Interoperability -- legislation & jurisprudence
United States
United States. Department of Health and Human Services

1676. Use of electronic health record data in clinical investigations

Publication:

Silver Spring, MD : Center for Drug Evaluation and Research, July 2018

Subject(s):

Clinical Trials as Topic
Electronic Health Records -- statistics & numerical data
Health Information Interoperability
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1677. Use of public human genetic variant databases to support clinical validity for genetic and genomic-based in vitro diagnostics: guidance for stakeholders and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, April 13, 2018

Subject(s):

Databases, Genetic
Reagent Kits, Diagnostic -- standards
Reproducibility of Results
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1678. Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff

Publication:

Silver Spring, MD : Center for Devices and Radiological Health, August 31, 2017

Subject(s):

Equipment and Supplies
Equipment Safety
Evidence-Based Medicine
Product Surveillance, Postmarketing
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

1679. 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

1680. Use of serological tests to reduce the risk of transmission of Trypanosoma cruzi infection in blood and blood components

Publication:

Silver Spring, MD : Center for Biologics Evaluation and Research, December 2017

Subject(s):

Blood Donors
Chagas Disease -- blood
Chagas Disease -- transmission
Disease Transmission, Infectious -- prevention & control
Donor Selection
Serologic Tests
Trypanosoma cruzi
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration