Author:
Tudur Smith Catrin,Stocken Deborah D.,Dunn Janet,Cox Trevor,Ghaneh Paula,Cunningham David,Neoptolemos John P.
Publisher
Public Library of Science (PLoS)
Reference15 articles.
1. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. ICH Harmonised Tripartite Guideline: Guideline for Good Clinical Practice E6(R1) 1996.
2. Clinical Trials Transformation Initiative (CTTI). Effective and Efficient Monitoring as a Component of Quality. Available: https://www.trialstransformation.org/projects/effective-and-efficient-monitoring/. 2012 Oct 1.
3. Monitoring the quality of conduct of clinical trials: a survey of current practices;BW Morrison;Clin Trials,2011
4. Bakobaki JM, Rauchenberger M, Joffe N, McCormack S, Stenning S, et al.. (2012) The potential for central monitoring techniques to replace on-site monitoring: findings from an international multi-centre clinical trial. Clin Trials. 9(2) 257–64.
5. The role of biostatistics in the prevention, detection and treatment of fraud in clinical trials. Statistics in medicine;GS Buyse M,1999
Cited by
56 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献