Instructions: Research the ethical and legal concerns of clinical research in the Kingdom of Saudi Arabia. 

What aspects of clinical research design helps to protect the human subjects? What are the best practices of creating an informed consent? 

Finally, create an informed consent form and include all the components that you have found are necessary to protect the patient.

Please use one of your references to support your informed consent components.

Your presentation should meet the following structural requirements:

  • Consist of 9 slides, this does not include the title and reference slides Keep bullet points to 3-5 words in the slides.
  • Each slide must provide detailed speakers notes—a minimum of 100 words and include your discussion in the speaker notes, explaining your findings for each slide .
  • Speaker Notes must use and cite relevant reference materials to support for your statements from a minimum of six scholarly articles.
  • follow APA writing format.