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Investigational New Drug Application
Subject Areas on Research
Building a drug development database: challenges in reliable data availability.
New FDA breakthrough-drug category--implications for patients.
The Food and Drug Administration and pragmatic clinical trials of marketed medical products.
The quantity and quality of worldwide new drug introductions, 1982-2003.
Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities.
t⁴ workshop report. Nanotoxicology: "the end of the beginning" - signs on the roadmap to a strategy for assuring the safe application and use of nanomaterials.
