WebCitiBusiness ® Online. CitiBusiness. Online. CitiBusiness Online is Citi’s banking platform for US-based Commercial Bank clients. Get real-time visibility into your global accounts … WebNov 9, 2024 · training, good clinical practice, research human subject protection, informed consent, institutional review board, IRB, sponsor, trial, study, investigator
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WebInvestigators* who started after June 1, 2016 must take a specific CITI GCP-ICH course ("Group 5") that contains three additional Emory-specific modules. Must be refreshed every three years while working on clinical trial(s). Additional information about training requirements per research role can be viewed in Required Training (PDF). WebOn the Main Menu screen, under the ‘University of Iowa Courses’ tab, in the ‘My Learner Tools for University of Iowa’ box, select the ‘Add a Course’ link. On the ‘Select Curriculum – University of Iowa’ screen, select the ‘ I am required to complete Good Clinical Practices (GCP) training’ option. Click the ‘Next’ button. device lock is disable http api may fail
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WebCITI Program GCP Training ICH E6 (R2) CITI Program’s GCP modules that reference ICH E6 were revised to reflect the Integrated Addendum to ICH E6 (R1): Guideline for Good … WebOptional CITI modules are available to all required to take CITI training. A list of modules available to UMMC faculty, staff, and students are as follows: Human Subjects Research (HSR) - IRB Chair Course. Good Clinical Practice (GCP) – GCP for Clinical Trials with Investigational Drugs (ICH Focus) – (Basic Course) WebCompletion of a CITI basic human subjects protections course is a prerequisite for taking the GCP course. GCP training is not a replacement for taking human subject training. GCP training must be renewed every three (3) years upon initial certification expiration, if the study team member is involved on an active clinical trial. device locked to ee