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Documents > food and drug administration
FDADocs 5/9/2008 | 0 (0) | 25 | 2 | 0 | English
CDER Forum for International Drug Regulatory Authorities
CDER's Office of Surveillance and Epidemiology
Kathleen Frost
Associate Director for Regulatory Affairs Office of Surveillance and Epidemiology Center for Drug Evaluation and Research - FDA
Outline
Overview of the Office of Surveillance and Epidemiology (OSE)
– Structure & Functions
Tools ... more>>
FDADocs 5/9/2008 | 0 (0) | 32 | 2 | 0 | English
FDADocs 5/9/2008 | 0 (0) | 56 | 2 | 0 | English
GovernmentDocs 5/4/2008 | 0 (0) | 54 | 2 | 0 | English
Safety Page
How FDA reviews drug names
Editors’ note: According to a 1999 Institute of Medicine report, approximately 7,000 deaths occur yearly due to medication errors. To help save lives, the Food & Drug Administration has agreed to share information on its drug error prevention activities with Drug Topics through this new quarterly column. What ... more>>
ProfessionalDocument 8/1/2008 | 0 (0) | 47 | 2 | 0 | English
ProfessionalDocument 8/1/2008 | 0 (0) | 24 | 2 | 0 | English
sammyc2007 4/28/2008 | 1 (1) | 78 | 2 | 0 | English
FDADocs 5/9/2008 | 0 (0) | 16 | 1 | 0 | English
Guidance for Industry on
Complementary and Alternative Medicine Products and Their Regulation by the Food and Drug Administration
DRAFT GUIDANCE
This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be submitted within 90 days of publication in the Federal Register of t ... more>>
GovernmentDocs 5/5/2008 | 0 (0) | 98 | 1 | 0 | English
FDA DRUG AND DEVICE PRODUCT APPROVALS
Volume 16 (1) January 1993
Center for Drug Evaluation and Research *George R. Scott (301) 443-3910 Center for Biologics Evaluation and Research Joseph Wilczek (301) 295-9012
Center for Devices and Radiological Health Mary Jo Robinson (301) 427-1186 Center for Veterinary Medicine Melanie R. Berson, D.V.M. (301 ... more>>
NTIA 6/30/2008 | 0 (0) | 69 | 1 | 0 | English
US-China Joint Commission on Commerce and Trade Medical Device and Pharmaceutical Subgroup Pharmaceutical Task Force Meeting August 30, 2005 Beijing, China Overview The Pharmaceutical Task Force under the U.S. – China Joint Commission on Commerce and Trade (JCCT) Medical Devices and Pharmaceuticals Subgroup met in Beijing, China on August 30, 2005. ... more>>
FDADocs 5/5/2008 | 0 (0) | 191 | 1 | 0 | English
Food and Drug Administration (FDA) Center for Drug Evaluation and Research (CDER) Joint Meeting of the Endocrinologic and Metabolic Drugs Advisory Committee (EMDAC) with the Advisory Committee for Pharmaceutical Science (ACPS) October 4, 2006
Meeting Participants
EMDAC Members in attendance (voting) Kenneth D. Burman, M.D. Thomas O. Carpenter, M.D ... more>>
FDADocs 5/9/2008 | 0 (0) | 59 | 1 | 0 | English
FDADocs 5/8/2008 | 0 (0) | 66 | 1 | 0 | English
GovernmentDocs 5/4/2008 | 0 (0) | 53 | 1 | 0 | English
Safety Page
Stemming drug errors from abbreviations
Problem: Abbreviations and tions that have been incorrectly ation for the investigational drug CPX, being tested in cystic fibrosis, acronyms save time; they can interpreted. Abbreviations and acronyms are sounds similar to CTX, which is also lead to medication errors. Not all practitioners inter ... more>>
sammyc2007 4/1/2008 | 0 (0) | 39 | 1 | 0 | English
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