Services

• Determining the type of research

• Determination of the universe and sample

• Determining the research hypothesis

• Determining the research design in accordance with the research hypothesis

• Detailed reporting of sample size calculation

• Creation of the randomization scheme

• Writing the statistical analysis plan

Statistical power analysis to be carried out within the scope of any study is generally done in two ways.

• Calculation of how many people the study will be conducted on, before proceeding to the data collection phase at the beginning of the study. This is known as a priori power analysis.

• Calculation of the power of the test used for the findings obtained after the study was completed. This is known as post-hoc power analysis. 

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However, before starting the study, it is very critical to determine the sample size at the planning stage.

• Choosing the most appropriate and up-to-date statistical analysis approach

• Univariate and multivariate tests

• Regression models

• Validity assessment methods of diagnostic tests

• Analysis of vital data

• Analysis of genetic data

• Analysis of scale development and adaptation of scales

• Other analyzes of data type and research hypothesis

• Writing research components such as research type, universe (population), sample

• Writing the randomization process

• Detailed writing of the sample size calculation that can meet the purpose of the study

• Writing the statistical analysis plan in detail and in accordance with the literature

​Supporting the findings with high quality tables and graphics increases the chance of publication of the study.

• Supporting the findings with the most appropriate tables and graphics

• Creation of accurate and striking tables

• Creation of accurate and striking graphics

We design and implement the required statistical examinations and tests, statistical verification procedures, and normative sampling plans in clinical studies and evaluations for medical devices in accordance with the Turkish Medicines and Medical Devices Agency and European Union legislation.