Question

According to federal regulations, an irb must have at least two community members to fulfill membership requirements; one member whose expertise is not in a scientific area and one member who is not affiliated with the institution.

Answer 1

What is the FDA's intention of having Institutional Review Boards strictly follow the regulations of 21 CFR 56?

The correct answer is the intention is to protect the rights and welfare of human subjects involved in investigations regulated by the FDA.

So C

Step-by-step explanation:

Answer 2

• IRB(Institutional Review Board)-

Mostly, FDA and HHS compose such committees to review the situations and activities in the various projects, which are held at different academic institutions and medical facilities for the purpose of scientific development. But to avoid any anti-human or any anti-life activity, while carrying out the process in the project these communities are composed to review there work. Theses committee can be renamed by the governing institutions as it all depends upon on the higher institutions to decide.These committees can also be named as the "Committee for the Protection of Human Subjects".

Step-by-step explanation:

• Importance of IRB:

It is very important for the federal institutions to keep and eye on the activities been carried out in the different research academies and schools. As for the reason that there are also some malicious ideas and activities been carried out lately which harmed many living beings in general, as to avoid any unethical activities during the different process of the projects, a review board is composed.