Abstract
A new European Union policy could increase the supply of legitimate pharmaceuticals in developing countries and thereby minimize the problem of counterfeit medicines, but many challenges remain. This paper describes the proposed European legislation and discusses its' potential strengths, weaknesses, opportunities and threats. Ultimately, we consider if the United States should consider similar policies.
Original language | English |
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Journal | Nature Biotechnology |
Volume | 37 |
Issue number | 1 |
Pages (from-to) | 21-22 |
Number of pages | 2 |
ISSN | 1087-0156 |
DOIs | |
Publication status | Published - 3 Jan 2019 |