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Consumer Fraud - FDA Information

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FDA Announces Actions to Strengthen its Postmarket Program for Medical Devices
The U.S. Food and Drug Administration (FDA) has announced its action plan for strengthening the way it monitors the safety of medical devices after they reach the marketplace.
CDER Reference Guide
Center for Drug Evaluation and Research Reference Guide General Information FDA ...
Consumer Education: Buying Medicine and Medical Products Over the Internet - Text/HTML version
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Division of New Drugs and Labeling Compliance (DNDLC)
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FDA Centennial at CDER: Milestones in Drug Regulation in the U.S.
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Guidance for Industry: Handling and Retention of BA and BE Testing Samples
Guidance for Industry Handling and Retention of BA and BE Testing Samples (PDF version of this document) ...
Statement of Steven K. Galson, M.D., M.P.H., Regarding Unapproved Prescription Drugs, June 8, 2006
Statement of Steven K. Galson, M.D., M.P.H., Regarding Unapproved Prescription Drugs, June 8, 2006 Good morning. As you?ve read in Dr. Von Eschenbach?s statement,...
CDER 2003 Report to the Nation
CDER Report to the Nation: 200 4 Table of Contents Print version ...
CDER Forum for International Drug Regulatory Authorities: September 25 - 28, 2006, Rockville, MD
CDER Forum for International Drug Regulatory Authorities September 25 - 28, 2006 Rockville, Maryland A program pamphlet and overview are also available in PDF format. ...
Ombudsman’s Annual Report for 2006
Ombudsman’s Annual Report for 2006 FDA, Center for Drug Evaluation and Research The CDER Ombudsman’s office serves as a portal for consumers, regulated...
Ombudsman Report 2004
Ombudsman?s Annual Report for 2004 FDA, Center for Drug Evaluation and Research The CDER Ombudsman?s office serves as a portal for consumers,...
Patient Misuse and Investigator Fraud in Clinical Trials
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Division of Drug Information: Relatd Drug Information Links
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