The war on drugs meets the war on pain nursing home patients caught in the crossfire : listening session before the Special Committee on Aging, United States Senate, One Hundred Eleventh Congress, second session, Washington, DC, March 24, 2010.Format: [microform] :
Publisher: Washington : U.S. G.P.O. :
Date: 2010. This title can be found in 2 Iowa libraries.
Preserve Access to Affordable Generics Act report together with minority views (to accompany S. 369) (including cost estimate of the Congressional Budget Office).Format: [electronic resource] :
Publisher: [Washington, D.C. : U.S. G.P.O.,
Date: 2010] This title can be found in 1 Iowa libraries.
The war on drugs meets the war on pain nursing home patients caught in the crossfire : listening session before the Special Committee on Aging, United States Senate, One Hundred Eleventh Congress, second session, Washington, DC, March 24, 2010.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2010. This title can be found in 1 Iowa libraries.
Guidance for industry format and content of proposed risk evaluation and mitigation strategies (REMS), REMS assessments, and proposed REMS modifications.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2009] This title can be found in 1 Iowa libraries.
Guidance for industry drug-induced liver injury, premarketing clinical evaluation.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2009] This title can be found in 1 Iowa libraries.
Proper disposal of prescription drugsFormat: [electronic resource] /
Publisher: Washington, D.C. : Office of National Drug Control Policy,
Date: [2009] This title can be found in 1 Iowa libraries.
Restoring FDA's ability to keep America's families safe hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Tenth Congress, second session, on examining the U.S. Food and Drug Administration, focusing on its ability to ensure the safety of food and the drug supply in the United States, April 24, 2008.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2009. This title can be found in 1 Iowa libraries.
Guidance for sponsors, industry, researchers, investigators, and Food and Drug Administration staff certifications to accompany drug, biological product and device applications/submissions : compliance with Section 402(j) of the Public Health Service Act, added by Title VIII of the Food and Drug Administration Amendments Act of 2007.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Policy :
Date: [2009] This title can be found in 1 Iowa libraries.
Guidance for industry SPL standard for content of labeling technical Qs & As.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2009] This title can be found in 1 Iowa libraries.
Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharmaceutical and device legislation hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, June 12, 2007.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2008. This title can be found in 1 Iowa libraries.
Guidance for industry providing regulatory submissions in electronic format : human pharmaceutical product applications and related submissions using the eCTD specifications.Format: [electronic resource] :
Publisher: Silver Spring, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research ;
Date: [2008] This title can be found in 2 Iowa libraries.
Guidance for industry E14 clinical evaluation of QT/QTc interval prolongation and proarrhythmic potential for non-antiarrhythmic drugs, questions and answers.Format: [electronic resource] :
Publisher: Silver Spring, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2008] This title can be found in 1 Iowa libraries.
Assessing the safety of our nation's drug supply hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 9, 2007.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2008. This title can be found in 1 Iowa libraries.
Drug Enforcement Administration's regulation of medicine hearing before the Subcommittee on Crime, Terrorism, and Homeland Security of the Committee on the Judiciary, House of Representatives, One Hundred Tenth Congress, first session, July 12, 2007.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2008. This title can be found in 1 Iowa libraries.
The Food and Drug Import Safety Act : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, on H.R. 3610, September 26, 2007.Publisher: Washington : For sale by the Supt. of Docs., U.S. G.P.O.,
Date: 2008. This title can be found in 1 Iowa libraries.
The Food and Drug Import Safety Act hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, on H.R. 3610, September 26, 2007.Format: [electronic resource] :
Publisher: Washington : U.S. G.P.O.,
Date: 2008. This title can be found in 1 Iowa libraries.
Guidance for industry providing regulatory submissions in electronic format, receipt date.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2007] This title can be found in 1 Iowa libraries.
Guidance for industry bioequivalence recommendations for specific products.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,
Date: [2007] This title can be found in 1 Iowa libraries.
Drug safety further actions needed to improve FDA's postmarket decision-making process : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /Format: [electronic resource] :
Author: Crosse, Marcia.
Publisher: [Washington, D.C.] : U.S. Govt. Accountability Office,
Date: [2007] This title can be found in 1 Iowa libraries.
This resource is supported by the Institute of Museum and Library Services under the provisions of the Library Services and Technology Act as administered by State Library of Iowa.