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P
Privacy by design
P
Processing
P
Processor
P
Profiling
P
Protocol
P
Pseudonymisation
P
Purpose limitation
R
Randomised Clinical Trials
R
Randomization and Trial Supply Management (RTSM )
R
Real-world data (RWD)
R
Real-world evidence (RWE)
R
Recipient
Record of processing activities
R
Restriction of processing
R
Right not to be subject to a decision based solely on automated processing
R
Right of access
R
Right of information
R
Right of rectification
R
Right to data portability
R
Right to erasure
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Term of the Day

Natural History Study

A natural history study is a preplanned intended to track the course of the disease. Its purpose is to identify demographic, genetic, environmental, and other variables (e.g., treatment modalities, concomitant medications) that correlate with the disease’s development and outcomes. Natural history studies are likely to include patients receiving the current standard of care and/or emergent care, which may alter some manifestations of the disease.

G

Good clinical practice (GCP)

Good clinical practice (GCP) means a set of detailed ethical and scientific quality requirements for designing, conducting, performing, monitoring, auditing, recording, analysing and reporting clinical trials ensuring that the rights, safety and well-being of subjects are protected, and that the data generated in the clinical trial are reliable and robust.