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Record if the subject will be continuing to the next trial period of this study.
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This is an example CRF used to collect protocol milestones, and informed consent.
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| title | aCRF: Protocol Milestones (e.g., Informed Consent) |
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In this study, subjects were randomized to a trial, which contain three epochs. A screening epoch, a product exposure epoch,, where subjects were required to use the tobacco product as described in the protocol, and a follow-up epoch. The Disposition Event CRF was collected at the end of each epoch of the trial. The sponsor may select the the Completion/Reason for Non-Completion terms from Controlled Terminology.
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In this study, subjects were randomized to a trial, which contain three epochs. A screening epoch, a product exposure epoch,, where subjects were required to use the tobacco product as described in the protocol, and a follow-up epoch. The Disposition Event CRF was collected at the end of each epoch of the trial. The sponsor may select the the Completion/Reason for Non-Completion terms from Controlled Terminology.
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| title | aCRF: Participation Disposition Event |
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Completion/Discontinuation Date
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This is an example of an SDTM dataset used to represent the data collected on the above example CRFs.
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