All marketed drugs and biologics are sold accompanied by the package leaflet (European Union [EU]) [1] or a package insert (Japan and the United States) [2–5], documents that describe product characteristics (active and inactive ingredients, chemical structure,...
CITATION STYLE
Wood, L. F. (2009). Investigator’s brochures. In Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics (pp. 105–119). Birkhäuser Basel. https://doi.org/10.1007/978-3-7643-8362-6_7
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