The purpose of this Support Center is to provide technical support, resources, tips, and answers to frequently asked questions regarding the CITI Program. We welcome contributions and feedback so please contact us with anything regarding the CITI Program or this Support Center.

Recently Added/Updated Content

Review CITI Program's new and updated content released this year.


Export Compliance (EC)


New EC modules cover distance education and the use of technology in research. Both modules are available for no additional fee to subscribing organizations

New EC Modules:

  • Export Compliance and Distance Education
  • Export Compliance When Using Technology in Research

Demo EC | Visit EC Catalog | Add Modules (no additional fee)


Good Clinical Practice (GCP)

On 15 December 2016, the International Council for Harmonisation (ICH) adopted the Integrated Addendum to ICH E6 (R1): Guideline for Good Clinical Practice E6 (R2), which reflects the evolving modernization of research (such as, increases in globalization, study complexity, and technological capabilities of clinical trials). After the ICH GCP E6(R2) guideline was adopted, CITI Program’s GCP modules that reference ICH E6 were revised to reflect the updated guideline. These GCP modules now specifically refer to the current guideline.

Updated GCP Courses:

DEMO GCP | View GCP Catalog


sIRB Use and Administration (HSR)

Three new modules on compliance with the requirement and expectation for use of a single Institutional Review Board (sIRB) for multi-site research are now available for no additional fee to subscribing organizations. These modules cover relying on a sIRB, serving as a sIRB of record, and authorization agreements.
 

New sIRB Modules:

  • When Relying on a sIRB
  • When Serving as a sIRB of Record
  • Authorization Agreements

DEMO HSR | View HSR Catalog | Add Modules (no additional fee)
Data and Safety Monitoring Module (HSR)

Identifying the need for a Data Safety Monitoring Board (DSMB) is essential to ensuring clinical trial data is acquired safely and legally. It is also important to differentiate the roles of the DSMB and Institutional Review Board (IRB) with regard to the protection of human subjects.  A new data safety and monitoring module is now available for no additional fee to subscribing organizations.

New Data and Safety Monitoring Module:
 
  • Data and Safety Monitoring in Human Subjects Research

DEMO HSR | View HSR Catalog | Add Modules (no additional fee)

Family Educational Rights and Privacy Act (FERPA) (IPS)

Provides a comprehensive course on FERPA's core aspects to ensure compliance with the law as well as role-specific material for a variety of professionals working in education and research.

New FERPA Modules in IPS:
 
  • FERPA: An Introduction
  • FERPA for Researchers
  • FERPA for Educational Administrators
  • FERPA for Instructors
  • FERPA for IRBs
  • FERPA for Students


DEMO IPS | View IPS Catalog | Add Modules (no additional fee)


Back to April 2017 Newsletter

Last Updated: Apr 24, 2017 02:10PM EDT

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