Storing biological samples from participants for future research.
Archives: Glossary Terms
approval (IRB/ethics)
Official decision by an ethics committee to allow a research study involving human participants to begin.
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study feasibility
How likely it is that a study can be completed.
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Serious Adverse Event (SAE)
A health issue that happens during a study and leads to hospital care, lasting medical problems, life-threatening conditions, or death.
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repository (research)
procedures (for participants)
The activities that participants will be asked to do during the research study.
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post-market surveillance
Continuing to collect and analyze information about the risks and benefits of medicine and devices after they have been approved for patient use.
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pilot study
A small study that is done to test a process before starting a larger study.
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minor
Someone considered too young to give legal consent.
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master protocol
An overall research plan that guides sub-studies that have their own research questions.
