The Food and Drug Administration approves more cancer drugs and those it approves receive approval more quickly than its European counterpart, according to a study published in Health Affairs by the advocacy group Friends of Cancer Research.
Released June 16, the study found that “contrary to repeated public assertions … new oncology medicines are consistently available in the United States before they are in Europe and they are more likely to be approved by the FDA than by the EMA [European Medicines Agency].”
Between 2003 and 2010, the median time for FDA’s cancer-drug approvals was six months while the EMA ...
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