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Pharmacokinetics / Pharmaceutical industry / Clinical research / Bioequivalence / Generic drug / Bioavailability / Food and Drug Administration / Clinical trial / Pharmaceutical drug / Abbreviated New Drug Application


Investigator Responsibilities in Protecting Participants in the Conduct of Bioequivalence Studies Cecilia C. Maramba, MD, MScID
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Document Date: 2010-02-19 02:38:05


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File Size: 450,71 KB

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