Assignment
1. Introduction
2. Research the ethical and legal implications of clinical research in the Kingdom of Saudi Arabia.
3. Understand international principles and guidelines which have to be followed when performing clinical trials
4. What aspects of clinical research design helps to protect the human subjects?
5. Name key principles of ethical considerations during clinical research and development
6. Discuss ethical concerns for designing, conducting and reporting the results obtained through the conduct of clinical trials
7. What are the best practices of creating an informed consent?
8. Create an informed consent and include all the components that you have found are necessary to protect the patient.
9. Conclusion.
Format your assignment according to the following formatting requirements:
1. The answer should be typed, double spaced, using Times New Roman font (size 12), with one-inch margins on all sides.
2. The response also include a cover page containing the title of the assignment, the student's name, the course title, and the date. The cover page is not included in the required page length.
3. Also Include a reference page. The Citations and references should follow APA format. The reference page is not included in the required page length.
Attachment:- References.rar