Which of the following are common activities of an HRPP or IRB office?

The selection of assisting investigators with protocol submissions as a common activity of a Human Research Protection Program (HRPP) or Institutional Review Board (IRB) office is spot on because this function is essential in ensuring that research studies are designed with participant safety and ethical standards in mind. This support typically includes guiding researchers through the submission process, helping them understand regulatory requirements, and providing resources to ensure that all necessary information is included for review. This assistance is crucial, especially for researchers who may be new to the process or unfamiliar with specific regulatory guidelines.

Moreover, while the other activities listed can also be associated with HRPP or IRB offices, they may not be as universally recognized or as direct in supporting researchers as the submission assistance. For example, making exempt determinations of studies is a specific assessment that may not encompass the broader support role an HRPP or IRB plays in assisting with the entire research submission process. Conducting audits of research data typically falls under post-approval monitoring and quality assurance, which, while important, is less about initial study support. Providing administrative support for meetings, while necessary for operational functions, does not directly involve engagement with the research protocol submission process itself. Therefore, assisting investigators with protocol submissions reflects a fundamental element of HRPP