A response to strategy #2: streamlining the regulatory process
- PMID: 16447137
- DOI: 10.1086/499594
A response to strategy #2: streamlining the regulatory process
Abstract
Regulatory burden has contributed to the decline in the production of vaccines in the United States. Production of influenza virus vaccine is perilously limited at a critical period when vulnerable populations are increasing and the threat of a pandemic is looming. Regulatory bodies must work with manufacturers to facilitate implementation of new production practices, to ensure steady expansion of the supply of safe and effective vaccines.
Comment on
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The United States Food and Drug Administration and the end of antibiotics.Clin Infect Dis. 2002 Feb 1;34(3):420-2. doi: 10.1086/338976. Clin Infect Dis. 2002. PMID: 11774094 No abstract available.
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