Preprints (not yet peer-reviewed)

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The FDA adaptive trial design guidance (1) is a thoughtful but lengthy document that explains on 50 pages wide-ranging and important topics “such as ... what aspects of adaptive design trials (i.e., clinical, statistical, regulatory) call for special consideration,...

["Clinical Trials","Drugs and Devices","Statistics"]
doi:10.7287/peerj.preprints.1825v1
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A PeerJ Preprint is a draft of an article, abstract, or poster that has not yet been peer-reviewed for formal publication. Submit a draft, incomplete, or final version of your work for free.

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