Sentence examples for exemption from consent from inspiring English sources

Exact(1)

Element 3 of the document includes detailed guidance as to the factors to consider when determining whether or not a research project should receive exemption from consent for secondary use of personal information.

Similar(58)

There are also a number of exemptions from consent for medical research that exist in law, such as public health surveillance.

Canadian federal and provincial data protection laws allow for exemptions from consent for research purposes where, among other conditions: (a) the research cannot be achieved without using personal information, and (b) it is impracticable to obtain consent [ 7].

Although consent is required for the collection of personal information from participants for medical procedures, medical examinations, and clinical trials, exemption from requiring consent may be appropriate for studies using medical records owing to impracticability of informed consent and the possibility of introducing biased study results.

The Emory University Institutional Review Board approved this study and granted an exemption from informed consent requirements, given the minimal risk nature of the study and the infeasibility of obtaining informed consent from individual patients for > 1.7 million billing records.

Exemption from informed consent was granted as this was a retrospective study with no identifying data.

The study was approved by the University of Oklahoma Health Sciences Center Human Research Protection Program as analysis of secondary data with an exemption from informed consent.

An exemption from written consent was obtained for the study and no incentives were offered for participation.

For patients included retrospectively, an exemption from informed consent was approved by the local Privacy and Data Protection Officer.

These require community consultation, public notification, and independent data and safety monitoring to allow exemption from informed consent [ 25- 28].

An exemption from patient consent at baseline (in-hospital stay via chart review) has been granted, as patients will be acutely ill and will require sedatives and pain killers making obtaining informed consent at that stage impossible.

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