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临床试验
制作一个有效的,成功◆的临床试验研究涉及深入的,精心的策划。花时间提前确保一个试验旨在维护参与者和实现其经济目标。这个网站包括了一个讨论的设计和对那些参与临床试验管理:
协议的概述,包括创建它们的相关的困难。
病例报告形式描述和设计考虑。
数据管理任务,以及策略创建干净的数据。
数据校正行为所需的数据验证和纠正数据。
入口点加上临床试验软件
入口点加上临床试验软件是设计来创建、部署和管理应用程序定制的临床试验。它使用一▲个先进的、可伸缩的、多线程的客户机-服务器网络体系结构与ODBC接口与SQL数据库,必须与远程站点进行临床试验。
An introduction to clinical trials and clinical trials software considerations, with references to more detailed information, and including a 21 CFR Part 11 checklist. Advantages of electronic data capture over paper. Description of Entrypoint Plus® clinical trials software.
Clinical Trials
Crafting an efficient, successful clinical trials study involves thorough, meticulous planning. Time well spent up front ensures a trial designed to safeguard participants and achieve its goals economically. This site includes a discussion of design and management concerns for those involved in clinical trials:
Protocols overview, including difficulties associated with creating them.
Case Report Forms description and design considerations.
Data Management tasks, as well as strategies for creating clean data.
Data Reconciliation actions required for verifying and correcting data.
Entrypoint Plus Clinical Trials Software
Entrypoint Plus clinical trials software is designed for creating, deploying, and administering custom clinical trial applications. It uses an advanced, scalable, multi-threaded client-server network architecture with ODBC to interface with SQL databases, a must for clinical trials with remote sites.
The Entrypoint Plus software comes with a set of electronic case report form templates with fields for demographics, medical history, examination data, adverse reactions, and lab tests. Entrypoint Plus supports remote data entry, batch compare, data export, a full audit trail, and sophisticated security options.
Try out the product. Evaluate Entrypoint Plus clinical trials software for 30 days without obligation.