Skip Navigation
Search
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 |