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Subjects (1-50 of 52)
United States Food And Drug Administration Rules And Practice
1
ElectronicResource GovDoc
 

Antibiotics FDA needs to do more to ensure that drug labels contain up-to-date information : report


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2012] 2012

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 Axe Federal Documents Online  GA 1.13:GAO-12-218    ---  Available
2
Electronic Book
 

Antibiotics, FDA has encouraged development, but needs to clarify the role of draft guidance and dev


United States. Government Accountability Office, author.
[Washington, D.C.] : United States Government Accountability Office, 2017. 2017

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 Axe Federal Documents Online  GA 1.13:GAO-17-189    ---  Available
3
ElectronicResource GovDoc
 

Bottled water FDA safety and consumer protections are often less stringent than comparable EPA prote


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-09-610    ---  Available
4
Electronic Book
 

Challenges for the FDA the future of drug safety : workshop summary


Symposium on the Future of Drug Safety: Challenges for the FDA (2007 : Washington, D.C.)
Washington, DC : National Academies Press, c2007. 2007

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 Axe ProQuest E-Book  Electronic Book    ---  Available
5
Print Material
 

COVID-19: federal efforts accelerate vaccine and therapeutic development, but tranparency needed on


United States. Government Accountability Office, author.
[Washington, D.C.] : United States Government Accountability Office, 2020. 2020

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-21-207    ---  Available
6
ElectronicResource GovDoc
 

A delicate balance FDA and the reform of the medical device approval process : hearing before the Sp


United States. Congress. Senate. Special Committee on Aging.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., U.S. G.P.O., 2011. 2011

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 Axe Federal Documents Online  Y 4.AG 4:S.HRG.112-92    ---  Available
7
ElectronicResource GovDoc
 

Dietary supplements FDA may have opportunities to expand its use of reported health problems to over


United States. Government Accountability Office, author, issuing body.
[Washington, D.C.] : United States Government Accountability Office, 2013. 2013

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-13-244    ---  Available
8
ElectronicResource GovDoc
 

Dietary supplements FDA should take further actions to improve oversight and consumer understanding


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-09-250    ---  Available
9
Electronic Book
 

Drug manufacturing : FDA should fully assess its efforts to encourage innovation : report to congres


United States. Government Accountability Office, author.
Washington, DC : United States Government Accountability Office, 2023. 2023

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 Axe Federal Documents Online    ---  Available
10
ElectronicResource GovDoc
 

Drug safety better data management and more inspections are needed to strengthen FDA's foreign drug


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2008] 2008

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 Axe Federal Documents Online  GA 1.13:GAO-08-970    ---  Available
11
ElectronicResource GovDoc
 

Drug safety FDA has begun efforts to enhance postmarket safety, but additional actions are needed :


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-10-68    ---  Available
12
ElectronicResource GovDoc
 

Drug safety FDA has conducted more foreign inspections and begun to improve its information on forei


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2010] 2010

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 Axe Federal Documents Online  GA 1.13:GAO-10-961    ---  Available
13
Electronic Book
 

Drug safety, FDA has improved its foreign drug inspection program, but needs to assess the effective


United States. Government Accountability Office, author.
[Washington, D.C.] : United States Government Accountability Office, 2017. 2017

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 Axe Federal Documents Online  GA 1.13:GAO-17-143    ---  Available
14
Electronic Book
 

Drug shortages, certain factors are strongly associated with this persistent public health challenge


United States. Government Accountability Office, author.
[Washington, D.C.] : United States Government Accountability Office, 2016. 2016

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-16-595    ---  Available
15
ElectronicResource GovDoc
 

FDA advisory committees process for recruiting members and evaluating potential conflicts of interes


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2008] 2008

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-08-640    ---  Available
16
Electronic Book
 

FDA food facility registry.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2009. 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-02-08-00060    ---  Available
17
Electronic Book
 

FDA food safety inspection.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 1991. 1991

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-05-90-01070    ---  Available
18
Electronic Book
 

FDA is issuing more postmarketing requirements, but challenges with oversight persist.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2016. 2016

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-01-14-00390    ---  Available
19
Electronic Book
 

FDA refusals of imported food products by country and category, 2005-2013


Bovay, John, author.
[Washington, D.C.] : United States Department of Agriculture, Economic Research Service, 2016. 2016

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 Axe Federal Documents Online  A 93.73/2:151    ---  Available
20
Electronic Book
 

FDA regulation of blood and blood products : recent draft guidance on donor eligibility


Sussman, Jared S., author.
[Washington, D.C.] : Congressional Research Service, 2023- 2023

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Location Call No. OPAC Message Status
 Axe Federal Documents Online    ---  Available
21
Electronic Book
 

FDA to consider whether and how to lower permissible nicotine levels in cigarettes


Barry, Matthew B., author.
[Washington, D.C.] : Congressional Research Service, 2018- 2018

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Location Call No. OPAC Message Status
 Axe Federal Documents Online    ---  Available
22
ElectronicResource GovDoc
 

FDA user fees 2012 issues related to accelerated approval, medical gas, antibiotic development, and


United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, author.
Washington : U.S. Government Printing Office, 2013. 2013

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.C 73/8:112-126    ---  Available
23
ElectronicResource GovDoc
 

FDA user fees 2012 how innovation helps patients and jobs : hearing before the Subcommittee on Healt


United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, author.
Washington : U.S. Government Printing Office, 2013. 2013

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.C 73/8:112-136    ---  Available
24
Electronic Book
 

FDA warning letters : timeliness and effectiveness.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 1999. 1999

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-09-97-00381    ---  Available
25
Electronic Book
 

FDA warning letters : trends and perspectives.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 1999. 1999

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-09-97-00380    ---  Available
26
Electronic Book
 

FDA warns of youth epidemic of e-cigarette use, faces regulatory challenges


Green, Victoria R., author.
[Washington, D.C.] : Congressional Research Service, 2018- 2018

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Location Call No. OPAC Message Status
 Axe Federal Documents Online    ---  Available
27
Electronic Book
 

FDA's independent evaluation of its food safety programs


Nair, Amber D., author.
[Washington, D.C.] : Congressional Research Service, 2023- 2023

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 Axe Federal Documents Online    ---  Available
28
Print Material
 

FDA's mammography inspections : while some problems need attention, facility compliance is growing :


United States. General Accounting Office.
Washington, D.C. : The Office, 1997. 1997

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 Axe Archives Fed Docs  GA 1.13:HEHS-97-25    ---  Available
29
Electronic Book
 

FDA's monitoring of postmarketing study commitments.


United States. Department of Health and Human Services. Office of Inspector General, author.
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2006. 2006

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 1.75:OEI-01-04-00390    ---  Available
30
Print Material
 

Federal "right-to-try" legislation : legal considerations


Staman, Jennifer A., author.
[Washington, D.C.] : Congressional Research Service, 2018- 2018

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 Axe Federal Documents Online  LC 14.25:LSB 10115/    ---  Available
31
ElectronicResource GovDoc
 

Federal rulemaking improvements needed to monitoring and evaluation of rules development as well as


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-09-205    ---  Available
32
ElectronicResource GovDoc
 

Food and Drug Administration approval and oversight of the drug Mifeprex : report to congressional r


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2008] 2008

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 Axe Federal Documents Online  GA 1.13:GAO-08-751    ---  Available
33
ElectronicResource GovDoc
 

Food and Drug Administration better coordination could enhance efforts to address economic adulterat


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2011] 2011

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 Axe Federal Documents Online  GA 1.13:GAO-12-46    ---  Available
34
ElectronicResource GovDoc
 

Food and Drug Administration overseas offices have taken steps to help ensure import safety, but mor


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2010] 2010

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 Axe Federal Documents Online  GA 1.13:GAO-10-960    ---  Available
35
ElectronicResource GovDoc
 

Food and Drug Administration response to heparin contamination helped protect public health; control


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2010] 2010

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 Axe Federal Documents Online  GA 1.13:GAO-11-95    ---  Available
36
ElectronicResource GovDoc
 

Food and Drug Administration's Critical Path Initiative : hearing before a subcommittee of the Commi


United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

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 Axe Federal Documents Online  Y 4.AP 6/2:S.HRG.110-293    ---  Available
37
ElectronicResource GovDoc
 

Food and Drug Administration's review process for products to treat rare diseases and neglected trop


United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies.
Washington : U.S. G.P.O., 2011. 2011

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.AP 6/2:S.HRG.111-841    ---  Available
38
ElectronicResource GovDoc
 

Food labeling FDA needs to better leverage resources, improve oversight, and effectively use availab


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2008] 2008

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 Axe Federal Documents Online  GA 1.13:GAO-08-597    ---  Available
39
ElectronicResource GovDoc
 

Food labeling FDA needs to reassess its approach to protecting consumers from false or misleading cl


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2011] 2011

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-11-102    ---  Available
40
Electronic Book
 

Food safety and the Food and Drug Administration : hearing before a subcommittee of the Committee on


United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies, author.
Washington : U.S. Government Publishing Office, 2022. 2022

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Location Call No. OPAC Message Status
 Axe Federal Documents Online    ---  Available
41
ElectronicResource GovDoc
 

Food safety agencies need to address gaps in enforcement and collaboration to enhance safety of impo


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-09-873    ---  Available
42
ElectronicResource GovDoc
 

Food safety FDA can better oversee food imports by assessing and leveraging other countries' oversig


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2012] 2012

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 Axe Federal Documents Online  GA 1.13:GAO-12-933    ---  Available
43
ElectronicResource GovDoc
 

Food safety FDA needs to reassess its approach to reducing an illness caused by eating raw oysters :


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2011] 2011

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 Axe Federal Documents Online  GA 1.13:GAO-11-607    ---  Available
44
ElectronicResource GovDoc
 

Food safety FDA should strengthen Its oversight of food ingredients determined to be Generally Recog


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2010] 2010

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 Axe Federal Documents Online  GA 1.13:GAO-10-246    ---  Available
45
ElectronicResource GovDoc
 

Food safety FDA's food advisory and recall process needs strengthening : report to congressional req


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2012] 2012

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 Axe Federal Documents Online  GA 1.13:GAO-12-589    ---  Available
46
ElectronicResource GovDoc
 

Food safety improvements needed in FDA oversight of fresh produce : report to congressional requeste


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2008] 2008

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  GA 1.13:GAO-08-1047    ---  Available
47
Electronic Book
 

Generic drugs : stakeholders views on improving FDA's information on patents : report to congression


United States. Government Accountability Office, author.
Washington, DC : United States Government Accountability Office, 2023. 2023

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 Axe Federal Documents Online    ---  Available
48
Electronic Book
 

Infant formula shortage : FDA regulation and federal response


Sheikh, Hassan Z., author.
[Washington, D.C.] : Congressional Research Service, 2022- 2022

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 Axe Federal Documents Online    ---  Available
49
ElectronicResource GovDoc
 

Innovation in America opportunities and obstacles : hearing before the Subcommittee on Competitivene


United States. Congress. Senate. Committee on Commerce, Science, and Transportation. Subcommittee on Competitiveness, Innovation, and Export Promotion.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2011. 2011

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.C 73/7:S.HRG.111-1018    ---  Available
50
ElectronicResource GovDoc
 

Medical devices FDA's approval of four temporomandibular joint implants : report to congressional re


United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2007] 2007

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 Axe Federal Documents Online  GA 1.13:GAO-07-996    ---  Available
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