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Office of Research Compliance Training Chart 

                    

What are You Doing? Training Requirement  Course Frequency
 Conducting Research CITI Responsible Conduct of Research Course Select the most appropriate course from the list One Time 
    Biomedical Sciences  
    Social and Behavioral Sciences  
    Humanities  
    Engineering  
    Interdisciplinary   
  CITI Conflict of Interest Course  Select the most appropriate course from the list At least once every four (4) years
    PHS/NIH Course  
    Non PHS/NIH Course   
Conducting Research and  the above training and then as applicable below    
Human Subjects  CITI Human Subjects Protection Course  Select the most appropriate course from the list Once every three years
    Social or Behavioral  
    Biomedical   
    Data or Specimens Only (do not work directly with human subjects)  
Study is NIH Funded Clinical Trial or GCP training is required by the study sponsor CITI Good Clinical Trial Practices Course The first course listed here (Good Clinical Practices Course) satisfies this requirement, but you can choose from others on the list if desired. Once every three years
    Good Clinical Practice Course (US FDA Focus)  
    GCP Course for Trials with Investigational Drugs (International/ICH Focus)  
    GCP Course for Clinical Trials Involving Investigational Medical Devices (International Focus)  
You are "on file" AS A Research Coordinator through the SOM's Office of Clinical Trials CITI Clinical Research Coordinator Course   One time 
Human Stem Cells CITI Human Stem Cells Course   One time
Animals  CITI Laboratory Animal Welfare Course Basic Course for Investigators, staff and students One time (unless species being studied changes) 
  Completion of Division of Occupational, Environmental, and Clinical Preventive Medicine Compliance for All Individuals Listed on Applications and Registration Form   One Time
  Complete the Mandatory DLAR Introduction to the Division of Laboratory Animal Resources   One Time
  Review all Standard Procedures that pertain to the research you are doing before you begin your research activities.  The procedures are listed in the application.   One Time
  Familiarize yourself with SBU, DLAR and Federal Policies   One Time 
Recombinant and/or Synthetic Nucleic Acid Molecule Read and Understand    
  Overview of the NIH Guidelines    One Time
  IBC Investigator Responsibilities   One Time  
  Environmental Health & Safety Training    Contact EH&S 
  ELS 002:  Lab Safety - Chemical Hazards    
  ELS 003:  Lab Safety - Biological Hazards    
  ELS 003:  Lab Safety - Biological Hazards    
    ENV 005: Regulated Waste Management    
    EOS 004:  Bloodborne Pathogens    
Controlled Substances No formal training requirement    
Radioactive Drugs No formal training requirement    
Any International Activities (includes activities inside and outside the U.S.)     Export Compliance for Researchers:  Part I   One Time
  Export Compliance for Researchers:  Part II   One Time
    As  applicable to your activities One Time
    Export Compliance and Distance Education  
    Export Compliance and Biosafety  
    Export Compliance for International Shipping  
    Export Compliance and Purchasing  
    Export Compliance and International and Foreign Waters  
    Export Compliance and Collaborations  
    Export Compliance and United States Sanctions Programs  
    Export Compliance When Using Technology in Research