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C
Clinical Outcome Assessment (COA)
C
Clinical Study
C
Clinical Trial
C
Clinical Trial Phases
C
Clinical Trial Site
C
Clinical Trials Information System (CTIS)
C
Clinical research
C
Clinician-reported outcome (ClinRO)
C
Consent
C
Controller
C
Cookies
C
Croos-border processing
D
Data Protection Impact Assessment (DPIA)
D
Data Protection Representative (DPR)
D
Data concerning heath
D
Data minimization
D
Data monitoring committee (DMC)
Data protection authority
D
Data protection by Default
D
Data protection by Design
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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.

P

Purpose limitation

Purpose limitation is a fair information practices principle, part of the original OECD Guidelines, and a piece of many privacy and data protection regulations such as the GDPR. 

The purposes for which personal data are collected should be specified no later than at the time of data collection and the subsequent use of that personal data is limited to the fulfillment of those purposes or such others as are not incompatible with those purposes and as are specified to the individual on each occasion of change of purpose, or for which there is a further legal basis that would not require notification.