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C
Clinical Outcome Assessment (COA)
C
Clinical Study
C
Clinical Trial
C
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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.

R

Right of information

The right of information refers to the information which shall be provided to a data subject whether or not the data have been obtained from the data subject.

The information which must be provided relates to the identity of the controller, the purpose(s) of the processing, the recipients, as well as the existence of the right of access to data and the right to rectify the data.

The right of information for the person concerned is limited in some cases, such as for public safety considerations or for the prevention, investigation, identification and prosecution of criminal offences, including the fight against money laundering.

In the context of processing operations within the EC institutions (see Articles 15 and 16 of Regulation (EU) 2018/1725), this right is often fulfilled by a privacy statement.

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