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At the recommendation of the treating clinician who will seek permission from the participant or authorised surrogate to be approached by the investigator, the investigator/s will seek informed consent or assent from potential trial participants or authorised surrogate.
For subjects who were deemed by the clinician not to have the capacity to give consent, a legally authorised surrogate provided consent.
The research protocol must state that consent to remain in the research should be obtained from the individual, or a legally authorised surrogate, as soon as possible.
This will occur through a verbal presentation of the written consent document, which the participant or authorised surrogate would then be given sufficient time to consider before consenting to the study or not.
At recruitment, every participant will be informed of the protocol of the study, and then he/she or his/her authorised surrogate will be asked to sign the consent form.
Similar(55)
Its replacement was authorised in 1956.
Not authorised.
Who authorised it?
A word not well authorised.
And who authorised its publication?
Had Lee authorised its publication?
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CEO of Professional Science Editing for Scientists @ prosciediting.com