Informed Consent Content and Process Requirements Trailer

The web seminar presents in an interactive environment, the elements of the informed consent document, and the components of the process. Industry specific scenarios are presented to reinforce important concepts, for example: evaluating and documenting capacity to consent, voluntariness, when a HIPAA authorization required, withdrawal of consent and more. Discussions also include reported poor regulatory performance regarding informed consent, and successful solutions for practices that increase the protection of human subjects in clinical research

Category:

Science & Technology

Tags:

• Clinical Research
• Informed Consent