Physicians’ Trust in the FDA’s Use of Product-Specific Pathways for Generic Drug Approval

Author:

Kesselheim Aaron S.,Eddings Wesley,Raj Tara,Campbell Eric G.,Franklin Jessica M.,Ross Kathryn M.,Fulchino Lisa A.,Avorn Jerry,Gagne Joshua J.

Funder

U.S. Food and Drug Administration

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference46 articles.

1. Food and Drug Administration. Fact Sheet: New User Fees for Generic Drugs Will Enhance Americans' Access to less Expensive Drugs and Generate Major Cost Savings. Aug 17, 2012. Available: http://www.fda.gov/RegulatoryInformation/Legislation/SignificantAmendmentstotheFDCAct/FDASIA/ucm310992.htm.

2. Services CfMaM National Health Expenditures 2013 Highlights.

3. Potential savings from substituting generic drugs for brand-name drugs: medical expenditure panel survey, 1997–2000;JS Haas;Ann Intern Med,2005

4. Physician perceptions about generic drugs;WH Shrank;Ann Pharmacother,2011

5. Clinical equivalence of generic and brand-name drugs used in cardiovascular disease: a systematic review and meta-analysis;AS Kesselheim;JAMA,2008

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