DAIDS Protocol Registration Policy and Manual e-Learning Modules
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.
Protocol Registration System Training
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 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 or staff at your site 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.
Protocol Registration Policy & Manual Training
Training is also available on the DAIDS PR Manual and Policy. This training focuses on the current PR requirements and how to implement the PR policy as described in the Manual. Compliance with the PR Policy is required as of 01 November 2010. This training is currently available as a pre-recorded 2 hour webinar session and as an e-learning module. To access the pre-recorded webinar, click here . To find this e-learning module on the DAIDS LMS, enter "protocol registration: policy and manual training" into the "Catalog" field.
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Last update: Wednesday, January 25, 2012
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