. In a clinical trial, part of the end requires submitting patient data to determine the effectiveness of the trial at a certain time and date. At a certain point the sponsor no longer submits patient data regarding their research; this is called a data lock. ("Bio-definitions," 2012) 2. true 3. Three reasons that adverse events are collected in clinical trials are: 1. Adverse events could result in termination or a drug or a change in dosage. A change in protocol may be needed. 2. Adverse events could affect the ethical soundness of a study. 3. To inform investigators and sponsors of these risks so ...
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