Sentence examples for User-friendly dosing from inspiring English sources

Exact(1)

Both approaches seem to exhibit some complementarity: a retrospective development of a model and, on the other hand, a clinical prospective validation of a nomogram, respectively.> To the best of our knowledge, the study by Pea et al. is the only to provide and validate two user-friendly dosing nomograms for the treatment of critical ill patients with vancomycin by CI [ 18].

Similar(59)

Incorporation of all variables will be used to develop a user-friendly antibiotic dosing algorithm.

All components of the system, such as the SLM, shutter and EMCCD camera, were controlled by a user-friendly software (Labview 8.5) for sequential doses performed in the optoinjection experiments as well as for optical trapping experiments.

The database classifies it in terms of significant variables, such as radiation quality, dose, dose rate and sampling timing, as to provide user-friendly tools to facilitate data integration and comparison.

To address this, work is currently ongoing to convert the NONMEM-model into a user-friendly tool for a priori and a posteriori dose predictions in both children and adults.

Overall, the results provided evidence that the once-daily rivastigmine patch offers a user-friendly treatment alternative to achieve higher patient compliance and dose escalation for better outcomes.

These user-friendly search tools enable the users to search for the database by gene name, dose quality, dose range and sampling time.

Effective PST or PSM requires not only able and motivated patients, a user-friendly, intelligent Electronic Patient Record and a suitable algorithm for management of dose adjustment, but also depends on reliable and accurate point of care testing devices.

In this application note, we describe the development and availability of a user-friendly software tool that integrates these standard methods in the analysis of microarray dose-response data.

We present in this paper a user-friendly software for the design and analysis of these Bayesian Phase I (resp. phase II) dose-ranging Clinical Trials (BPCT).

The aim of this study was to develop and validate a simple and user-friendly nomogram to predict 24 hour trough concentrations reliably across a range of gestational ages, allowing modification of the dose at the earliest opportunity.

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