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Essentials for Regulatory Specialists: A new virtual workshop

CTSI is now offering a virtual workshop that provides training for University of Minnesota research professionals, such as regulatory specialists, research coordinators, project managers, who are new to taking on a regulatory role in human research studies.


The workshop covers:

  • The role and responsibilities of a regulatory specialist
  • The regulations that define their role 
  • Creating consent forms and other essential study documents 
  • Maintaining a regulatory binder 
  • IRB submissions

This a four-hour training over two days. 


To take the course, participants must complete the following required training prior to attending: :

  • HIPAA training
  • CITI training - Good Clinical Practice (GCP) and Human Research Protections for Biomedical Study Teams training or Social/Behavioral or Humanist Research Investigators and Key Personnel

Take the course

The course will be offered quarterly, and is available for self-registration through the University of Minnesota’s Training Hub. 

Access the training