Browsing by Subject "Government Regulation"
Now showing items 1-3 of 3
-
Collective action and individual choice: rethinking how we regulate narcotics and antibiotics.
(J Med Ethics, 2013-12)Governments across the globe have squandered treasure and imprisoned millions of their own citizens by criminalising the use and sale of recreational drugs. But use of these drugs has remained relatively constant, and the ... -
Compliance with results reporting at ClinicalTrials.gov.
(N Engl J Med, 2015-03-12)BACKGROUND: The Food and Drug Administration Amendments Act (FDAAA) mandates timely reporting of results of applicable clinical trials to ClinicalTrials.gov. We characterized the proportion of applicable clinical trials ... -
Data monitoring and interim analyses in the pharmaceutical industry: ethical and logistical considerations.
(Stat Med, 1993-03)The characteristics of data monitoring and the need for the use of data monitoring committees in clinical trials sponsored by the pharmaceutical industry differ from those of trials sponsored by government. Data monitoring ...
