Informed Consent in Clinical Research

Informed Consent in Clinical Research

This course will enable participants to have an understanding of the background and practical implications of the valid informed consent process. The knowledge and understanding gained, coupled with practical examples is intended to give participants the confidence to take a proactive role in the consent process back in the workplace.

This is a professionally developed course essential for anyone working within clinical research

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What you will learn

• This course will enable participants to have an understanding of the background and practical implications of the valid informed consent process.

Rating: 4.04545

Level: Beginner Level

Duration: 31 mins

Instructor: Linda Hopkinson