DAIDS Protocol Registration (PR) Registration System

Protocol Registration (PR) is the process by which DAIDS confirms and tracks Clinical Research Site (CRS) compliance with NIAID (DAIDS) policies, institutional review board (IRB) requirements, and U.S. federal regulations for research involving human subjects. PR also enables DAIDS to collect regulatory documents associated with investigator qualifications and responsibilities and confirm that site-specific informed consent forms comply with U.S. regulations and appropriate guidelines.

Training is now available on the DAIDS PR System (DPRS) via the DAIDS Learning Management System (DAIDS LMS). This training reviews how to submit PR documents via the web-based DPRS. Staff who are responsible for preparing, tracking, monitoring and/or submitting documents for PR and who have never had DPRS training are required to obtain training on this system before using it. However, staff who have already had DPRS training are not required to get additional DRPS training.

Trainees must have a DAIDS LMS account to access this self-directed e-learning module. If you do not have a DAIDS LMS account, click here to request one. To locate this training in the DAIDS LMS, after you log in, enter "DRPS" in the Search Catalog field at the top of the screen.

For problems or questions about:

• The DPRS web based system, contact DAIDS ES Support.
• Protocol Registration System Training, contact the DAIDS CRS Training Team.
• Protocol Registration submission, contact DAIDS PR Office