DAIDS Required Courses
|DAIDS Clinical Research Policies eLearnings|
|Become familiar with the DAIDS Clinical Research Policies using one of our eLearning courses. You can take these courses in addition to or in place of reviewing the policies themselves.|
|Introduction to Quality Management|
|Develop a basic understanding of quality management and how to implement a quality culture at clinical research sites.
|DAIDS Adverse Experience Reporting System (DAERS)|
|This course will train CRS staff on how to assess Adverse Events using the Manual for Expedited Reporting of Adverse Events to DAIDS, gain access to the DAIDS Adverse Experience Reporting System (DAERS), and report EAEs to DAIDS using DAERS.
|Human Subject Protection (HSP) / Good Clinical Practice (GCP)|
|Identify the training requirements and the means by which the requirements can be met for human subjects protection. There are three options for meeting the requirement.|
|Clinical Site Monitoring (CSM) System|
|Engage in this interactive course featuring case studies designed for new personnel and helpful tips to refresh current CSM users. Clinic and pharmacy staff members who will be interacting with the monitors and addressing monitoring issues in the CSM must take this course.
|DAIDS Protocol Registration System (DPRS)|
|Learn to use the online protocol registration repository to upload and track submission documents and reports. Staff members who will use the system to prepare, submit, and track protocol registration documents must take this course.