Informed Consent in Clinical Research

What you’ll learn
  • This course will enable participants to have an understanding of the background and practical implications of the valid informed consent process.
Requirements
  • This course is for anyone working within clinical research and involved in the consent process
Description

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.

Who this course is for:
  • Anyone working within clinical research and involved in the consent process
    REDEEM CODE

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