Phase 1 Clinical Trials Lead Author(s): Bernard Lo, M.D. Selection of Participants in Phase 1 Clinical Trials In Phase 1 clinical trials, a common ethical and design ...
What Makes Some Research "Minimal Risk?" Lead Author(s): Bernard Lo, M.D. The concept of minimal risk plays a pivotal role in the federal regulations concerning ...
What Do Regulators Classify as "Research"? Lead Author(s): Bernard Lo, M.D. The federal regulations define research as a "systematic investigation designed to develop ...
Using Placebo Controls Lead Editor : Bernard Lo, M.D. A placebo control is acceptable if no effective therapy exists for the condition being studied. However, if ...
Ethical Issues of Research In Developing Countries Lead Author(s): Bernard Lo, MD Research in resource poor countries is essential in order to develop affordable treatments ...
Data Monitoring in Clinical Trials Investigators commonly have questions regarding data and safety monitoring plans (DSMPs) in clinical trials. The Committee on Human ...
Clinical Research Ethics Educational Materials WELCOME to the Clinical Research Ethics Educational Materials web on the CTSpedia. The Clinical Research Ethics ...
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