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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
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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 Representative (DPR)

The data protection representative (DPR) is the EU representative of non-EU controllers that are not established in the EU (do not have an affiliate). A DPR is mandatory, if the processing in the EU is:

  • On a large scale
  • Of special categories of data (such as sensitive data)
  • Relating to criminal convictions and offences
  • Results in a risk to the rights and freedoms of natural persons, taking into account the nature, context, scope and purposes of the processing