Ethics in Medical Research

This course is designed for beginners who are new to medical research or who have limited knowledge of research ethics and IRBs. Participants will be equipped with the knowledge and skills needed to conduct ethical research and submit protocols for IRB review.

It provides a comprehensive overview of the ethical issues involved in medical research and the role of IRBs in ensuring the protection of human subjects. This course is essential for anyone involved in medical research, including researchers, study coordinators, and members of IRBs. Upon completion of this course, Participants will be able to make better decisions related to ethical issues in medical research, such as ensuring informed consent is obtained from study participants, maintaining privacy and confidentiality of study participants, and ensuring the safety of study participants.

Overall, participants who complete this course will be better equipped to conduct ethical medical research and ensure the protection of human subjects, which is essential for advancing scientific knowledge and improving healthcare outcomes.

Topics Covered:

• Introduction to Medical Research Ethics
• Ethical Issues in Medical Research
• Regulations and Guidelines for Medical Research
• Outline of Good Clinical Practice (GCP) guidelines.
• Role of Institutional Review Boards (IRBs)
• IRB Review Process
• Informed Consent and Its Importance
• Case Studies in Medical Research Ethics

What will you learn from this course

• Understanding of Ethics in Medical Research
• Knowledge of Regulations and Guidelines
• Awareness of Ethical Issues
• Understanding of IRBs and Their Role
• Ability to Conduct Ethical Research
• Better Decision Making