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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.

D

Data protection by Default

Data protection by Default is the implementation of appropriate technical and organisational measures for ensuring that, by default, only personal data which are necessary for each specific purpose of the processing are processed. That obligation applies to the amount of personal data collected, the extent of their processing, the period of their storage and their accessibility. In particular, such measures shall ensure that by default personal data are not made accessible without the individual's intervention to an indefinite number of natural persons. Such organizational measures could consist, inter alia, of minimising the processing of personal data, pseudonymising personal data as soon as possible, transparency with regard to the functions and processing of personal data, and enabling the data subject to monitor the data processing.

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