Sample Essay on:
Clinical Trial Budgeting

Here is the synopsis of our sample research paper on Clinical Trial Budgeting. Have the paper e-mailed to you 24/7/365.

Essay / Research Paper Abstract

This 10 page paper looks at the way in which clinical trial budgets are created, assessing the different stages and the various types of cost. The paper presents information which will provide a solid foundation for the creation and assessment of clinical trial budgets. The bibliography cites 7 sources.

Page Count:

10 pages (~225 words per page)

File: TS65_TEclinbud.doc

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Unformatted sample text from the term paper:

due to the range and scope of the procedures that may give rise to costs. The budgeting process will need to take a number of different elements into account, including the type of patients and the way in which they will be brought into the trial, the type of trial and protocols, including the number visits, treatment and test costs, dealing with any potential complications, staff fees including coordinator and investigator fees, the time period over which the study will take place, and the area in which the study is taking place. For a clinical trial protocol testing the efficacy of a new asthma treatment the different aspects of the budgeting and the areas where costs will need to be assessed may be considered as a theoretical framework and consider how a framework may be developed to account for the costs. It is assumed that the trial is testing a treatment where the sample is either given the treatment being trialled or a placebo. The costs associated with the trials may be divided into two main categories; the direct costs incurred for each of the trial subjects and the overhead associated with the study (Gallin and Ognibene, 2007). In a trial to assess the efficacy of a treatment, where the difference tested for subjects is the difference between a treatment and a placebo the processes and costs will be the same for each patient. This means that budgeting can take place by assessing the cost on a per patient/subject basis and then multiply this for subject number the direct costs (Pierce, 2000). The way that modern trial protocols are designed seeks to balance the need for reliable results based on scientific methods with recognition of the costs and practical aspects, by trying to achieve this with the minimum number ...

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