SAS® and Microsoft Excel® for Tracking and Managing Clinical Trial Data: Methods and Applications for Information DeliveryMicrosoft Excel is widely used in the pharmaceutical industry and therefore frequently requested due to familiarity and ease of use. This paper outlines an automated data ...
The clinical trial roadmap is a free PowerPoint template that features all the 3 main phases necessary for any drug or procedure to receive approval from the FDA. Phase I is conducted on a small, healthy group of participants and aims to determine the safe dosage as well as uncover potential...
Choose the objectiveFind the sample size, then select thenon-inferiority trialand thebinaryoutcome. Thealphais0.05. The desiredpoweris0.9.The% of success for the control groupis70%and the% of success for the treatment groupis75%. Thenon-inferiority limitis equal to 8%. Once you have clicked...
This free clinical trial data management audit checklist template will help you develop your own checklist. This Excel template lets you show the status of your audit in an easy color-coded display, the category and tasks to review, and what criteria you require. It brings all your audit requ...
Introduction Write three paragraphs to explain why the trial was necessary. At the end of the Introduction, state the research question(s) explicitly. For example:Therefore the research questions for this study were, in stroke patients able to walk independently:1.Does one month of treadmill ...
Import Data into MATLABImport Data into STATAImport Data into SPSSImport Data into ExcelExport AE/SAEExported Data FormatExported Data FilesHow to Export DataExporting Data in Greenlight Guru ClinicalForm level export Monitoring Data VerificationLock/Unlock Data EventQueriesReview Form AnswersReporting Data...
"I have worked with Yvanne Enever and the PHARMExcel team for several years on a complex, multicentre clinical trial. I have found them be efficient, highly professional while being accommodating and very supportive. I have worked with other clinical trial research organisations on similar studies...
Electronic sources (eSources) can improve data quality and reduce clinical trial costs. Our team has developed an innovative eSource record (ESR) system in China. This study aims to evaluate the efficiency, quality, and system performance of the ESR syst
If no template is yet available for this journal, please follow the format of the sample references and citations as shown in this Guide. If you use reference management software, please ensure that you remove all field codes before submitting the electronic manuscript. More information on how ...
This section provides general style and formatting information only. Formatting guidelines for specific article types can be found below. Research Reviews Editorials Letters to the Editor Research Letters Preparing additional files Back to top As the length and quantity of data is not restricted for ma...