Protocol Registration

About the DAIDS RSC Protocol Registration Office

The DAIDS RSC Protocol Registration Office (PRO) receives and processes all protocol registration materials submitted by Clinical Research Sites (CRSs) participating in DAIDS-supported and/or -sponsored clinical trials.  They work closely with the DAIDS Protocol Registration Team (PRT) to establish internal procedures and processes.

The DAIDS protocol registration process verifies that sites have received the necessary Institutional Review Board (IRB)/Ethics Committee (EC) and other applicable Regulatory Entity (RE) or Approving Entity approvals and have provided to DAIDS all documentation pertaining to investigator qualifications and responsibilities that are required by the U.S. Federal regulations and the National Institutes of Health (NIH). The DAIDS protocol registration process also verifies that site-specific informed consent forms contain the necessary information to comply with U.S. Federal regulations. 

Content last reviewed on 
February 1, 2018