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Informed Consent Process and Documentation

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Location

5142 Burton Wing - The Hub

Event description

Description

Learn best practices for obtaining and documenting initial and ongoing informed consent in clinical research,
including the roles of the legally acceptable representative and impartial witness. Although not impacted by the
changes to ICH GCP Topic E6, a revised template for documenting the informed
consent discussion will be introduced.

Intended Audience:

SickKids clinical research staff engaged in prospective clinical research studies/trials that require consent.

Date and Time

Location

5142 Burton Wing - The Hub

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