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- Cynthia F Kleppinger and Leslie K Ball.
- Division of Scientific Investigations, Office of Compliance, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
- Clin. Infect. Dis. 2010 Aug 1; 51 Suppl 1: S111-6.
AbstractThere is an increasing focus on having quality systems in place during the planning stages of clinical trials. Such systems require the development and implementation of standards for each step. Although this is not imposing something totally new on clinical research, a systematic approach will produce a more reliable and useful end product--high-quality data obtained without compromising the protection of human subjects' rights and welfare. A suggested quality system with standards for each step is addressed in this article.
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