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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.
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