先进的Oracle临床软件工具,用于临床研究从患者数据收集到数据库锁定

Vasanth kumar Kunithala, Ahamed Kabeer, Sateesh Kumar Vemula
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引用次数: 2

摘要

本文是基于Oracle临床软件工具在临床研究中的应用。众所周知,进行研究是一个昂贵而耗时的过程,因为它需要额外的人力资源,许多软件工具,以及对临床研究软件的全面了解。这种特殊的软件有助于提高试用性能并降低公司的成本。本文主要介绍了患者入组、数据录入、数据验证、E-data & SAE对账、编码、差异管理、质量控制流程和数据锁定等过程。制药行业采用不同的方法来收集、传输和存储患者数据。向参与跟踪的人员提供软件工具的知识将帮助他们简化工作。目的是通过使用适当的临床试验指南,提供Oracle临床软件工具的完整知识。这也为数据操作的职责和功能提供了一个完整的概念,以及工具分析,这也有助于处理风险概况。上述所有申请都将在提交FDA的同时提取患者的适当和一致的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advance Oracle Clinical Software tool used in clinical research from patient data collection to data base lock
Abstract This article is based on how the Oracle Clinical Software tool is used in clinical research. It is known that conducting research is a costly and time consuming process as it requires extra human resources, many software tools, and thorough knowledge of software in clinical research. This particular software helps in improving the trial performance and reduces the cost to the company. This article mainly describes the process of patient enrollment, data entry, data validation, E-data & SAE reconciliation, coding, discrepancy management, quality control process and data lock. Pharma Industries follow different methods for collecting, transferring, and storing patients data. Providing the knowledge of software tools to the persons who are involved in the trails will help them in simplifying their work. The objective is to provide complete knowledge of the Oracle Clinical Software tool by using proper guidelines of clinical trials. This also gives a complete idea of responsibilities and the functionality of data operation as well as tools analysis which would also help in tackling the risk profiles. All the above-mentioned applications would make one extract appropriate and consistent data of a patient, while submitting FDA.
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