RRT 110: Human Subjects Protection (HSP) Training

11 modules


Course Length
30 mins

Advarra University



Human Subjects Protection (HSP) training is essential for investigators and research staff. HSP training describes how investigators, sponsors, and IRBs work together to protect the rights, safety, and well-being of subjects on clinical trials. 

HSP training aims to ensure that:

  • the rights, safety, and well-being of human subjects are protected
  • privacy and confidentiality of human subjects in research are maintained

View each video to learn more about different topics in HSP.  To pass this course, you must complete the assessment with a score of 80% or greater. 

Attendance at this program has been approved for 1.00 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1.00 hours of CE credit.


  • What is Human Subjects Protection?
  • Why is it Important to Protect Subjects in Research?
  • Who is Responsible for Protecting Human Subjects?
  • What is the IRB's Role in Protecting Human Subjects?
  • What is Your Role in Protecting Human Subjects?
  • Privacy of Human Subjects
  • Confidentiality of Human Subjects
  • Safety Reporting
  • Biospecimens in Primary Research


By completing/passing this course, you will attain the certificate Advarra Completion Certificate (Expires)

What is HSP?
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Why is HSP Important?
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Who is Responsible for HSP?
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What is the IRB's role in HSP?
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What is Your Role in HSP?
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Privacy of Human Subjects
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Confidentiality of Human Subjects
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Safety Reporting
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Biospecimens in Primary Research
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HSP Further Reading Document
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HSP Assessment
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