药物和生物制品开发中的分散的临床试验
Ryan Robinson1, Leonard Sacks2
1U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Medical Policy, Silver Spring, MD, USA. Ryan.Robinson1@fda.hhs.gov.
分散临床试验 (DCT) 为参与者提供便利,但需要谨慎管理. 成功实施DCT取决于强有力的培训,监督和风险评估,以应对远程活动协调的挑战.
科学领域:
- 临床研究方法论临床研究方法论
- 监管科学是一种监管科学.
背景情况:
- 分散临床试验 (DCT) 涉及传统场所以外的试验活动.
- 美国食品和药物管理局 (FDA) 支持DCT以加强临床试验参与.
研究的目的:
- 突出DCT的好处和挑战.
- 为成功实施DCT提供指导.
主要方法:
- 对DCT概念和FDA立场的审查.
- 识别潜在的后勤和监管挑战.
- 强调风险管理策略.
主要成果:
- DCT为参与者提供方便和改进的访问.
- 挑战包括协调远程活动和监督委托任务.
- 积极的风险评估和管理至关重要.
结论:
- DCT为临床研究提供了一个有前途的模型.
- 有效实施需要通过培训和监督来解决协调和监督方面的挑战.
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