What procedures must be described in an agreement called an "assurance of compliance" with ohrp? procedures in place to ensure that the research complies with ethical principles (such as the world medical association’s declaration of helsinki). procedures in place that ensure that subjects will be protected in a manner commensurate with the common rule, including review by an independent committee comparable to an irb. procedures in place to outline how unanticipated problems will be reported to the local irb. procedures in place to outline how subjects will be randomized?

Respuesta :

The correct option is A.
For research that uses human subject as their specimens, the subject protection and regulation policies demands that researchers involved in such research must submit a written assurance of compliance to OHRP. The written assurance of compliance ensures that the necessary steps have been taken to follow ethical guidelines during the research process.

Answer;

-Procedures in place that ensure that subjects will be protected in a manner commensurate with the Common Rule, including review by an independent committee comparable to an IRB.

Explanation;

-HHS human subject protection regulations and policies necessitate that any institution that is involved in non-exempt human subjects research conducted or supported by HHS must submit a written assurance of compliance to OHRP.

- The Federalwide Assurance (FWA) is the only type of assurance of compliance accepted and approved by OHRP.