Glossary
Explore Our Glossary of Clinical Research Terms & Definitions.
Trial Monitoring
Ongoing review of trial activities to ensure compliance with protocol and regulations.
Quality Control
The process of ensuring that data collected in a clinical trial meets specified standards.
Trial Design
The structure and methodology of a clinical trial, including randomization, blinding, and endpoints.
Biobank
A repository for storing biological samples, such as blood or tissue, collected during a clinical trial.
Protocol Violation
A deviation from the approved trial protocol that may impact the study�s integrity.
Open-Label Study
A study in which both researchers and participants know the treatment being administered.
Investigator Meeting
A gathering of clinical trial investigators to discuss trial protocol and updates.
Safety Profile
A summary of a treatment�s known risks and side effects based on clinical trial data.
Independent Ethics Committee (IEC)
A group responsible for reviewing the ethical aspects of a trial.
Clinical Pharmacology
The study of drugs in humans, including absorption, distribution, metabolism, and elimination.
Statistical Analysis Plan (SAP)
A detailed plan outlining how data will be analyzed in a clinical trial.
Adherence Plan
A strategy to help participants follow trial protocols and treatment regimens.
Recruitment Challenges
Difficulties encountered in enrolling participants for a clinical trial.
Human Subject
An individual who participates in a clinical trial as a research participant.
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