Hint No. 1 – When completing your study’s continuing review form, please remember NOT to include with the form any document amendments you’re hoping to get approved. The IRB no longer reviews amended documents with continuing reviews, and hasn’t done so since we switched from ARIA to CLARA. In some cases, the IRB may have […]

When drafting your protocol, please pay close attention to how the subjects’ age range is described in the text. Different regulatory requirements apply to different ages, which is why the IRB may send contingencies asking you to be very, very specific when describing how old your participants are. For example, when we see an age […]

When completing a new submission form in CLARA, please pay close attention to the questions related to HIPAA and respond individually to each one. We understand that some of the questions may seem like forehead-slappers, such as a request to explain why access to the protected health information is necessary in a chart review study. […]

The IRB staff has noticed an uptick in recent weeks of IRB submissions describing projects that have already been completed. Fortunately, none of the projects in question met the regulatory definition of research requiring IRB review. However, please note that the IRB cannot review or approve projects that have already been completed. In fact, researchers […]

The Food and Drug Administration (FDA) has oversight over some, but not all, of the research that comes through the UAMS IRB. When submitting studies, please confirm that your consent and HIPAA authorization forms correctly reflect whether the FDA will have access to study records. Projects that involve FDA-regulated products such as investigational drugs and […]

The UAMS IRB requires all UAMS study staff engaged in research to complete human subject protection training once every three years. If you are new to UAMS from another institution, you may have already have done such training through citiprogram.org at your previous workplace.  To meet the UAMS training requirements, you might only have to […]

When typing in document names in CLARA, please keep the following points in mind: IRB letters pick up the document names you type in when listing approved items. If the names are complete and accurate, you’ll have clear documentation of the specific items approved.

Please note that the IRB does not require investigators to submit case report forms (CRFs) to the IRB for review. CRFs are designed to be specific to study sponsors’ data collection and analysis needs, and when they are submitted, the IRB does not review them closely. Also, submitting a CRF with a new submission has […]

Some studies do not require the investigator to obtain the formal written consent of subjects using an IRB-approved consent form. The circumstances in which documentation of consent can be waived are described in UAMS IRB Policy 15.3 (see section II.B). Please note, however, that even when a waiver of documentation of consent is requested/granted, some […]

CLARA allows researchers to add their CVs to their CLARA profiles, rather than requiring the CV to be uploaded as a document to individual protocols. Including the CV in the profile automatically links the CV with each of that person’s studies. This is a change from our old system; in ARIA, CVs had to be […]