APA format, 2 pages, 3 references, please complete the course and send results of course attached! Thanks
Discussion Question
Complete the NIH “Protecting Human Research Participants” course at: http://phrp.nihtraining.com. Include a copy of the certificate of completion and add to your post as an attachment for proof of completion. Once you have completed, respond to the following:
Share your reaction to this course. Next, research your workplace organization to find out how research is conducted that involves human participants. For example, is there an IRB or ethics committee? If so, do they review proposals? Next, find out the composition of the members and discuss if they meet federal guidelines.
Expert Solution Preview
Introduction:
The protection of human research participants is an essential aspect of medical research. As medical students, it is important to understand the ethical considerations involved in conducting research involving human participants. In this post, I will share my reaction to the NIH “Protecting Human Research Participants” course and discuss the process of conducting research at my workplace organization.
Answer:
Completing the NIH “Protecting Human Research Participants” course was an informative and eye-opening experience. The course effectively highlighted the ethical considerations and guidelines involved in conducting research involving human participants. It emphasized the importance of informed consent, confidentiality, and minimizing risks to the participants. The case studies presented in the course were particularly insightful and demonstrated the complex ethical dilemmas that researchers may face.
At my workplace organization, research involving human participants is conducted under the guidance of an institutional review board (IRB). The IRB is responsible for reviewing research proposals involving human subjects to ensure that they meet the ethical guidelines set forth by federal regulations. The composition of the IRB consists of members with diverse backgrounds, including physicians, scientists, community members, and ethicists. They meet the federal guidelines for an IRB composition, which mandates that the IRB include members who have expertise in various scientific, medical, and ethical fields.
In conclusion, the NIH “Protecting Human Research Participants” course and my research experience reflect the importance of ethical considerations and guidelines in conducting research involving human participants. It is crucial to uphold the rights and welfare of the participants and ensure that they are informed and protected throughout the research process. The presence of an IRB with diverse members and expertise is an important step towards achieving this goal.
