In place of an SOP, provide information from the manufacturer (e.g., user manual) as supplementary information with your ethics application.If the above criteria do not apply to your equipment or device and/or study procedure, then an alternative to an SOP can be provided. any other use of equipment or devices where the study procedure includes the possibility of injury, harm, or discomfort to a participant (e.g., EEG cap and gel, EMG/ECG electrodes, TMS, tDCS, etc.). a controlled act as outlined by the Regulated Health Professions Act of Ontario or.creation of a bio-bank or bio-repository, or. commercially produced equipment or devices that have been modified by the researchers, or are being used differently from the manufacturer's directions/terms of use, where there is the possibility of injury, harm, or discomfort to participants, or.equipment or devices that have been created and/or built by the researchers to collect bio-metric or physiological data, or. SOPs are to be included as part of the research ethics application when the research involves:
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