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But, by extending the PCROM information model we obtained a CRIM able to consider that in TRANSFoRm the EHR and CRF are not only data input interfaces but can also trigger the generation of reminders and initiate the distribution of invitations and alerts (in case of adverse events or overdosing) at defined time points on the study timeline (e.g. visits and appointments).
The study timeline is presented in Fig. 2.
The study timeline is presented in Figure 2.
The study timeline is shown in Figure 1.
The study timeline can be found in Figure 1.
The study timeline with milestones is reported in Figure 1.
Table 1 illustrates the study timeline.
Figure 1 shows the study timeline.
The study timeline was negatively affected by these various challenges.
Figure 2 shows the sampling and study timeline.
Several differences between this study and the original one, such as measurement differences, differences in study timeline, and analytic differences, make for difficult direct comparisons of the results.
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