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Global and national actions to prevent trade in substandard and adulterated medicines

Bibliographic Data

ID19592017
AuthorsRichard Wilder (0000-0002-7161-7484, University of New Hampshire, corresponding author), Sam Halabi (0000-0002-4603-8480, Georgetown University, corresponding author), Lawrence O Gostin (0000-0001-5286-4044, Georgetown University, corresponding author)
EditorsBashar Haruna Gulumbe (0000-0003-0642-6902)
Year2025
Volume5
Issue2
Pagese0004024
Publication date2025-02-20
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenuePLOS Global Public Health (JOURNAL)
Journal identifiersISSN: 2767-3375 • E-ISSN: 2767-3375
PublisherPublic Library of Science (PLoS) (PUBLISHER)
DOI10.1371/journal.pgph.0004024
PMID39977428
OpenAlexW4407765145
LanguageEN
References cited1

Recent mass-poisoning events caused by substandard medicines placed in global markets raise the question as to what more can be done to stop it. Efforts have been underway for years at the World Health Organization and other multilateral fora, such as the National Academies of Medicine in the U.S. While these efforts have led to improvements, several gaps remain which, unless addressed, will allow this problem in international trade to continue. Some countries have failed to implement the standards set by the WHO by not fully empowering national regulatory agencies to lead national efforts. Further, some countries do not fully exercise their responsibility under WHO standards to confirm that the information in documents accompanying internationally traded medicines is complete, accurate, and current. It is time to revisit international standards in this area to determine the causes of these problems and to address them

Access to medicines · Business · Developing country · Economic growth · Economics · International trade · Political science · World trade · Intellectual Property and Patents · Pharmaceutical Economics and Policy · Pharmaceutical Quality and Counterfeiting

Citation velocityhistorical
Highly citedNo
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