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Journal Article
J Health Polit Policy Law (2012) 37 (5): 779–814.
Published: 01 October 2012
..., Australia, and the United Kingdom — specifically, why Canada alone failed to adopt nationwide, public pharmaceutical insurance. It demonstrates that the pace of change has significant implications for the scope of policy development. It provides new mechanisms to explain why incremental reforms stall based...
Journal Article
J Health Polit Policy Law (2013) 38 (3): 505–544.
Published: 01 June 2013
...Denis G. Arnold; James L. Oakley As the pharmaceutical industry lobbies European regulators to permit direct-to-consumer advertising (DTCA) of prescription drugs in the European Union, we found that five leading companies violated industry-developed and -promulgated standards for ethical...
Journal Article
J Health Polit Policy Law (2022) 47 (5): 583–607.
Published: 01 October 2022
...Robin Feldman; Brent D. Fulton; Jamie R. Godwin; Richard M. Scheffler Abstract Context: Dramatic increases in pharmaceutical merger and acquisition (M&A) activity since 2010 suggest we are in the midst of a third wave of industry consolidation. Methods: The authors reviewed 168 economic, legal...
Journal Article
J Health Polit Policy Law (2024) 49 (1): 73–98.
Published: 01 February 2024
...Herschel Nachlis; Kyle Thomson Abstract Context: Regulatory approaches to COVID-19 vaccine authorizations varied substantially across countries. Facing a common public health threat, what accounts for regulatory variation? This study focuses on emergency pharmaceutical and vaccine regulatory...
Journal Article
J Health Polit Policy Law (2013) 38 (4): 735–755.
Published: 01 August 2013
...Bhaven N. Sampat; Tahir Amin The 1995 Trade Related Intellectual Property Rights (TRIPS) agreement required developing countries to grant product patents in pharmaceuticals. Developing countries have since explored various measures to ameliorate potential negative effects of the new laws on public...
Journal Article
J Health Polit Policy Law (1992) 17 (4): 847–868.
Published: 01 August 1992
...Louis H. Orzack; Kenneth I. Kaitin; Louis Lasagna The European Community (EC) plans to create a single market for pharmaceutical medicines, but the drug industry is closely linked to cultural and societal values concerning health; to the national regulatory agencies responsible for the evaluation...
Journal Article
J Health Polit Policy Law (2003) 28 (1): 109–132.
Published: 01 February 2003
...Ramón Castellblanch A comparison of the Vermont and Maine cases of attempting to control pharmaceutical prices in the year 2000 shows that the Maine legislators were more successful in challenging pharmaceutical industry political power. This comparison shows that challenging the industry...
Journal Article
J Health Polit Policy Law (2006) 31 (5): 1015–1019.
Published: 01 October 2006
.... Christopher Scott Harrison. The Politics of the International Pricing of Prescription Drugs. Westport, CT: Praeger, 2004. 224 pp. $65.95 cloth. Richard Henry Parrish II. Defining Drugs: How Government Became the Arbiter of Pharmaceutical Fact. New Brunswick, NJ: Transaction Books, 2003. 163 pp. $29.95...
Journal Article
J Health Polit Policy Law (2014) 39 (3): 691–705.
Published: 01 June 2014
... political and regulatory environment, this report explores pharmaceutical pricing options for Russia that balance greater access to medicines with achieving government plans of boosting local pharmaceutical production. To match innovative medicine prices with their health benefits, in the long run, we...
FIGURES
Journal Article
J Health Polit Policy Law (2016) 41 (2): 157–179.
Published: 01 April 2016
...Denis G. Arnold; Jennifer L. Troyer Abstract The pharmaceutical industry has been criticized for developing and aggressively marketing drugs that do not provide significant health benefits relative to existing drugs but retain the benefits of patent protection. Critics argue that drug marketing...
FIGURES
Journal Article
J Health Polit Policy Law (2009) 34 (6): 931–977.
Published: 01 December 2009
...John Abraham Coinciding with sixty years of the U.K. National Health Service (NHS), this article reviews the neglected area of the governance of the pharmaceutical industry and the NHS. It traces the relationships between the pharmaceutical industry, the state, and the NHS from the creation...
Journal Article
J Health Polit Policy Law (2019) 44 (5): 765–787.
Published: 01 October 2019
...Denis G. Arnold; James L. Oakley Abstract Context: Spending on direct-to-consumer advertising (DTCA) for prescription pharmaceuticals has risen to record levels, five times as much as in 1996 in inflation-adjusted dollars. Major health care provider organizations have called for additional...
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Journal Article
J Health Polit Policy Law (2024) 49 (2): 249–268.
Published: 01 April 2024
...Liam Bendicksen; Aaron S. Kesselheim; C. Joseph Ross Daval Abstract Context: The False Claims Act is the US federal government's primary tool for identifying and penalizing pharmaceutical fraud. The Department of Justice uses the False Claims Act to bring civil cases against drug manufacturers...
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Journal Article
J Health Polit Policy Law (2022) 47 (6): 629–648.
Published: 01 December 2022
...Pragya Kakani; Michael Chernew; Amitabh Chandra Abstract Context: To what extent does pharmaceutical revenue growth depend on new medicines versus increasing prices for existing medicines? Moreover, does using list prices, as is commonly done, instead of prices net of confidential rebates offered...
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Includes: Supplementary data
Journal Article
J Health Polit Policy Law (2022) 47 (6): 835–851.
Published: 01 December 2022
... manufacturer price pharmaceutical policy The Medicaid Drug Rebate Program (MDRP) was established in 1992 to mitigate the costs of states choosing to expand their Medicaid programs to include prescription drug coverage. The MDRP has, at its core, a trade-off between pharmaceutical manufacturers and state...
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Includes: Supplementary data
Journal Article
J Health Polit Policy Law (2022) 47 (6): 755–778.
Published: 01 December 2022
...Marc A. Rodwin Abstract This article compares the pharmaceutical pricing policies employed by public and private insurers in the United States with seven price and spending control strategies employed in the United Kingdom, France, and Germany. Differences between American and European policies...
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in Federal Enforcement of Pharmaceutical Fraud under the False Claims Act, 2006–2022
> Journal of Health Politics, Policy and Law
Published: 01 April 2024
Figure 1 Federal fraud settlements involving pharmaceutical manufacturers, 2006–2022. Source : US Department of Justice press releases.
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Image
in Federal Enforcement of Pharmaceutical Fraud under the False Claims Act, 2006–2022
> Journal of Health Politics, Policy and Law
Published: 01 April 2024
Figure 2 Totality of federal fraud settlement payments involving pharmaceutical manufacturers. Note : All values in January 2023 dollars. Source : US Department of Justice press releases.
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Journal Article
J Health Polit Policy Law (2018) 43 (1): 5–18.
Published: 01 February 2018
... will require close coordination among manufacturers, payers, and regulators. Copyright © 2018 by Duke University Press 2018 Medicaid best-price rule pharmaceutical pricing value-based payment outcome-based pricing Even in today's polarized political landscape, a consensus has emerged...
Journal Article
J Health Polit Policy Law (2016) 41 (3): 423–450.
Published: 01 June 2016
...Elize Massard da Fonseca; Francisco Inácio Bastos Abstract The protection of pharmaceutical intellectual property (IP) rights is one of the most controversial debates in contemporary public health as countries have to balance incentives for drug development with the necessity of providing life...
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