Pharmaceutical Affairs Act

Results: 118



#Item
31Medicinal chemistry / Clinical pharmacology / Quality / Quality by Design / Pharmaceuticals policy / Prescription Drug User Fee Act / QBD / Center for Drug Evaluation and Research / Office of Regulatory Affairs / Pharmaceutical sciences / Food and Drug Administration / Pharmacology

DIA 2014 50th Annual Meeting

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Source URL: www.fda.gov

Language: English
32Pharmaceutical sciences / Pharmaceutical industry / Pharmacology / ClinicalTrials.gov / Food and Drug Administration Amendments Act / Food and Drug Administration / Trials / Clinical trials registry / Clinical research / Research / Clinical trials

Clinical Trials Disclosure Henry Durivage, Pharm.D. Associate Director, Clinical Trials and Regulatory Affairs Yale Center for Clinical Investigation

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Source URL: ycci.yale.edu

Language: English - Date: 2014-11-11 08:53:57
33Pharmaceutical sciences / Medical device / Center for Devices and Radiological Health / Federal Food /  Drug /  and Cosmetic Act / Unique Device Identification / Office of Regulatory Affairs / Mammography Quality Standards Act / Premarket approval / Investigational Device Exemption / Food and Drug Administration / Medicine / Health

PDF Document

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Source URL: www.fda.gov

Language: English
34Pharmaceutical sciences / Medical device / Office of Regulatory Affairs / Prescription Drug User Fee Act / Federal Food /  Drug /  and Cosmetic Act / Center for Food Safety and Applied Nutrition / Health Canada / Unique Device Identification / Food safety / Food and Drug Administration / Medicine / Health

GLOSSARY OF GLOSSARY OF ACRONYMS

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Source URL: www.fda.gov

Language: English
35Clinical research / Vehicle inspection / Office of Regulatory Affairs / Inspection / Mammography Quality Standards Act / Medicinal chemistry / Food and Drug Administration / Pharmaceutical sciences / EIR

DOC Document

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Source URL: www.fda.gov

Language: English
36Pharmaceutical sciences / Pharmacology / Pharmaceuticals policy / Food law / Food safety / Federal Food /  Drug /  and Cosmetic Act / Office of Regulatory Affairs / Compounding / Form FDA 483 / Food and Drug Administration / Health / Medicine

Guidance for Industry Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug Inspection U.S. Department of Health and Human Services

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Source URL: www.fda.gov.

Language: English
37Pharmaceutical sciences / Prescription Drug User Fee Act / Center for Food Safety and Applied Nutrition / Food Safety Modernization Act / Federal Food /  Drug /  and Cosmetic Act / Office of Regulatory Affairs / Prescription medication / Food and Drug Administration / Health / Medicine

This document is scheduled to be published in the Federal Register on[removed]and available online at http://federalregister.gov/a[removed], and on FDsys.gov[removed]P DEPARTMENT OF HEALTH AND HUMAN SERVICES

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Source URL: s3.amazonaws.com

Language: English - Date: 2014-07-31 08:56:04
38Patient safety / Pharmaceutical sciences / Health / Medicine / Health Insurance Portability and Accountability Act / Pharmacology / Clinical pharmacology / Medical prescription

Everything you need to know about New Jersey Prescription BlanksĀ  DEADLINE EXTENDED: November 2, 2014 The Division of Consumer Affairs granted a final extension

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Source URL: www.acog.org

Language: English - Date: 2014-10-02 11:45:14
39Pharmaceuticals policy / Pharmaceutical sciences / Pharmacology / Food law / Therapeutics / Prescription Drug User Fee Act / Food Safety Modernization Act / Center for Food Safety and Applied Nutrition / Office of Regulatory Affairs / Food and Drug Administration / Health / Medicine

[removed]Federal Register / Vol. 79, No[removed]Friday, August 1, [removed]Notices domestic FDF facility fee of $247,717. The foreign FDF facility fee is $15,000

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Source URL: www.gpo.gov

Language: English - Date: 2014-10-06 16:33:50
40Health / Medicine / Food law / Pharmacology / Prescription Drug User Fee Act / New Drug Application / Federal Food /  Drug /  and Cosmetic Act / Pharmaceutical industry / Food and Drug Administration / Pharmaceuticals policy / Pharmaceutical sciences

Alan Goldhammer, PhD Associate Vice President, US Regulatory Affairs

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Source URL: www.fda.gov

Language: English - Date: 2004-11-05 15:26:13
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