Food and Drug Administration Amendments Act

Results: 135



#Item
41GAO[removed]Highlights, DRUG SAFETY: FDA Has Conducted More Foreign Inspections and Begun to Improve Its Information on Foreign Establishments, but More Progress Is Needed

GAO[removed]Highlights, DRUG SAFETY: FDA Has Conducted More Foreign Inspections and Begun to Improve Its Information on Foreign Establishments, but More Progress Is Needed

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Source URL: www.gao.gov

Language: English - Date: 2011-09-29 08:45:25
42Alphabet Blocks and Chalkboard

Alphabet Blocks and Chalkboard

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Source URL: www.fda.gov

Language: English
43ABC COMPANY (ALL CAPS & BOLD)

ABC COMPANY (ALL CAPS & BOLD)

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Source URL: www.fda.gov.

Language: English
44Pediatric Drug Development: Regulatory Expectations BASIC

Pediatric Drug Development: Regulatory Expectations BASIC

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Source URL: www.fda.gov

Language: English
45Inclusion of Certain Devices Within the Accredited Persons Program – Third Party Review of Clinical Data _________________________________________________

Inclusion of Certain Devices Within the Accredited Persons Program – Third Party Review of Clinical Data _________________________________________________

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Source URL: www.fda.gov

Language: English
46FY 2013 MDUFA Financial Report

FY 2013 MDUFA Financial Report

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Source URL: www.fda.gov

Language: English
47FY 2013 MDUFA FINANCIAL REPORT REQUIRED BY THE MEDICAL DEVICE USER FEE AMENDMENTS OF 2013

FY 2013 MDUFA FINANCIAL REPORT REQUIRED BY THE MEDICAL DEVICE USER FEE AMENDMENTS OF 2013

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Source URL: www.fda.gov

Language: English
48SOPP 8402: Designation of Amendments as Major Version #4 Effective Date: October 1, 2012 I. Purpose This Standard Operating Policy and Procedure (SOPP) describes the policy and procedures for

SOPP 8402: Designation of Amendments as Major Version #4 Effective Date: October 1, 2012 I. Purpose This Standard Operating Policy and Procedure (SOPP) describes the policy and procedures for

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Source URL: www.fda.gov

Language: English
49Lost Prescription Drug Savings from Use of REMS Programs to Delay Generic Market Entry The Law The Food and Drug Administration Amendments Act of[removed]FDAAA) gave FDA the authority to require a Risk Evaluation and Mitig

Lost Prescription Drug Savings from Use of REMS Programs to Delay Generic Market Entry The Law The Food and Drug Administration Amendments Act of[removed]FDAAA) gave FDA the authority to require a Risk Evaluation and Mitig

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Source URL: www.gphaonline.org

Language: English - Date: 2014-07-23 14:14:54
501701 K Street, PnoNE[removed]NW, Suite[removed]

1701 K Street, PnoNE[removed]NW, Suite[removed]

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Source URL: www.fda.gov

Language: English - Date: 2006-01-03 18:15:55