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Trial Information: Adjunct Prof. Dr. Kim Yu is Program Vice President at R. Gruner & Associates. He is an Advisor to Dr. Tom Barrett-Harney, Chairman and Managing Partner at R. Martin Heiser. Download This course is designed to explain the basic concepts that will be utilized by a successful trial prep to provide the trialists with information and strategies which will help to develop their initial research and clinical practice. Results of a scientific research based clinical trial would include statistical analyses, risk changes, and other, in-depth information which will be utilized to explain the findings in primary trial trials. In order to conduct a clinical trial, the clinical trialists needs to have the complete materials and procedure for entering and evaluating the trial elements and their critical outcomes in primary trials, including these elements, and to have the opportunity to thoroughly evaluate the elements and evaluate the most optimal outcome from the trial. Other essential elements of a primary trial: conduct the trial in advance and assess the results using the latest available testing technology, such as the latest in-house systems, the latest computer hardware, and the latest in-house software. Additionally, conduct a thorough scientific analysis of the results of the trial. Other essential elements of a secondary trial: carry out clinical protocols, including a detailed blood sample preparation, critical evaluations using the latest in-house testing technology, the latest system software, new system hardware, and new information about the included materials and protocols. Additional Resources Needed Please read the instructions on the PRB page above to the extent possible, and any additional information you may need with regard to the above procedure (Click here for more information). This course will focus on the use of the current findings in primary trials using the methodology developed by Dr. Tom Barrett-Harney (see course info).[1]. A successful primary trial results (over the period of approximately two years) should be divided into core (N) and secondary (P) trial elements which can include risk behavior and clinical management problems, as determined by the use of the latest available resources by the investigators. The first core test can be conducted in the trial at the end of the primary trial and the secondary test can be conducted as indicated by the use of the latest available equipment, such as the latest in-house testing technology, the latest visual technology used, and the latest in-house testing software