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A supportive patient is:

Investigators have how long to notify the sponsor of serious adverse effects?

More than half of the research sites are now located:

True or False:  The FDA requires more elements in an informed consent than does the International Conference on Harmonisation (ICH) guidelines.

Which of the following regarding publication bias is true:

Traditional descriptive epidemiology focused on disease patters in relation to:

What issue arises when shifting research studies overseas to vulnerable populations?

The clinical Trials Registry requires all medical doctors to register with the FDA.

The main reason that women were excluded from the Multiple Risk Factor Intervention Trial (MRFIT) was:

Which of the following events lead to ethical developments in clinical research?