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There are some important reasons why low- and middle-income countries (LMICs) may choose to make greater use of competition law and policy to reduce the cost of treatment. First, multilateral trade rules allow substantial flexibility in the development and application of competition law and...
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In this chapter, we make a first attempt at exploring the intersection where sustainable finance, fintech, and competition law and policy meet. We find that fintech can ensure that sustainable finance goes beyond greenwishing and avoids greenwashing, while at the same time supporting increasing...
Persistent link: https://www.econbiz.de/10014254783
One of the most difficult legal issues today involves settlements by which brand-name drug companies pay generic firms to delay entering the market. Such conduct requires courts to consider not only patent and antitrust law, but also the Hatch-Waxman Act, the complex regime governing behavior in...
Persistent link: https://www.econbiz.de/10013100789
The Supreme Court's decision in FTC v. Actavis has received widespread attention for its antitrust analysis of settlements by which brand-name drug companies pay generics to delay entering the market. Much of the attention has focused on the continued enforcement of these “reverse payment”...
Persistent link: https://www.econbiz.de/10013073468
The generic industry lobby, Association for Accessible Medicines (“AAM”), often represents the public interest. In the pharmaceutical industry, it challenges brand drug companies' anti-competitive conduct. It fights for lower prices for consumers. And it has built up goodwill for its work in...
Persistent link: https://www.econbiz.de/10012832925
As part of the FDA's hearing on "The Hatch-Waxman Amendments: Ensuring a Balance Between Innovation and Access," I offer testimony that does two things.First, it shows how the balance has tilted away from generic access, pointing as examples to settlements, product hopping, REMS patents, and...
Persistent link: https://www.econbiz.de/10012951817
Two principles collide in the pharmaceutical industry. On the one hand, the U.S. Food and Drug Administration (“FDA”) approves potentially dangerous drugs under Risk Evaluation and Mitigation Strategies (“REMS”) programs when a drug's benefits outweigh its risks. But on the other hand,...
Persistent link: https://www.econbiz.de/10012953068
Rising drug prices are in the news. By increasing price, drug companies have placed vital, even life-saving, medicines out of the reach of consumers. In a recent development, brand firms have prevented generics even from entering the market. The ruse for this strategy involves risk-management...
Persistent link: https://www.econbiz.de/10012955066
One of the tools brand-name drug companies have used to delay generics involves the filing of questionable citizen petitions with the FDA. This short comment applauds the agency for addressing this pressing issue and offers modifications that would make the proposed guidance stronger.The FDA can...
Persistent link: https://www.econbiz.de/10012909240