CE Certified Modules for the HSR Basic Course
- Page Views 136144
| 1 | Belmont Report and CITI Course Introduction | 1127 |
| 2 | History and Ethics of Human Subjects Research (revised 5/17) | 498 |
| 3 | Basic Institutional Review Board (IRB) Regulations and Review Process | 2 |
| 4 | Informed Consent | 3 |
| 5 | Social and Behavioral Research(SBR) for Biomedical Researchers | 4 |
| 6 | Records-Based Research | 5 |
| 7 | Genetic Research in Human Populations | 6 |
| 8 | Populations in Research Requiring Additional Considerations and/or Protections | 16680 |
| 9 | Research Involving Prisoners | 8 |
| 10 | Research Involving Children | 9 |
| 11 | Research Involving Pregnant Women, Human Fetuses, and Neonates | 10 |
| 12 | Avoiding Group Harm - U.S. Research Perspectives | 14080 |
| 13 | Avoiding Group Harms - International Research Perspectives | 14081 |
| 14 | FDA-Regulated Research | 12 |
| 15 | Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or others in in Biomedical Research | 14777 |
| 16 | Research and HIPAA Privacy Protections | 14 |
| 17 | History and Ethical Principles - SBE | 490 |
| 18 | Defining Research with Human Subjects - SBE | 491 |
| 19 | The Regulations - SBE | 502 |
| 20 | Assessing Risk - SBE | 503 |
| 21 | Informed Consent - SBE | 504 |
| 22 | Privacy and Confidentiality - SBE | 505 |
| 23 | Research with Prisoners - SBE | 506 |
| 24 | Research with Children - SBE | 507 |
| 25 | Research in Public Elementary and Secondary Schools - SBE | 508 |
| 26 | International Research - SBE | 509 |
| 27 | Internet-Based Research - SBE | 510 |
| 28 | Unanticipated Problems and Reporting Requirements in Social and Behavioral Research | 14928 |
| 29 | Cultural Competence in Research | 15166 |
| 30 | I Have Agreed to Be an IRB Community Member, Now what? | 13018 |
| 31 | International Studies | 971 |
| 32 | Students in Research | 1321 |
| 33 | The IRB Member Module - "What Every New IRB Member Needs to Know" | 816 |
| 34 | Vulnerable Subjects - Research Involving Workers/Employees - | 483 |
| 35 | Stem Cell Research Oversight (Part I) | 13882 |
| 36 | Stem Cell Research Oversight (Part II) | 14584 |
| 37 | Conflicts of Interest in Human Subjects Research | 17464 |
| 38 | Consent and Biobanks and Associated Databases | 17254 |
| 39 | Consent and Cultural Competence | 17263 |
| 40 | Informed Consent and Incidental Findings in Research with Human Subjects | 17342 |
| 41 | Consent and Subject Recruitment Challenges: Remuneration | 16881 |
| 42 | Consent and Subject Recruitment Challenges: Therapeutic Misconception | 17259 |
| 43 | Consent in the 21st Century | 17060 |
| 44 | Consent Tools Used by Researchers | 16944 |
| 45 | Consent with Subjects Who Do Not Speak English | 17260 |
| 46 | External IRB Review | 16711 |
| 47 | The IRB Administrator's Responsibilities | 13813 |
| 48 | Data and Safety Monitoring in Human Subject Research | 17433 |
| 49 | Illegal Activities or Undocumented Status in Human Research | 16656 |
| 50 | Humanitarian Use Devices (HUDs) (ID: 13306) | 16306 |
| 51 | Ethical and Practical Considerations in Community-Engaged Research (CEnR) | 16996 |
| 52 | Single Institutional Review Board (sIRB) Use and Administration: When Relying on a sIRB | 17387 |
| 53 | Single Institutional Review Board (sIRB) Use and Administration: When Serving as a sIRB of Record | 17388 |
| 54 | Single Institutional Review Board (sIRB) Use and Administration: Authorization Agreements | 17392 |
| 55 | Phase I Research: Understanding Phase I Research | 16873 |
| 56 | Phase I Research: Protecting Phase I Subjects | 16874 |
| 57 | Gender and Sexuality Diversity (GSD) in Human Research | 16556 |
| 58 | Research Involving Subjects at the End of Life | 16658 |
| 59 | Research with Critically Ill Subjects | 16592 |
| 60 | Research with Decisionally Impaired Subjects | 16610 |
| 61 | Research with Older Adults | 16502 |
| 62 | Research with Persons who are Socially or Economically Disadvantaged | 16539 |
| 63 | Research with Subjects with Physical Disabilities & Impairments | 16657 |
| 64 | FERPA: An Introduction | 17407 |
| 65 | FERPA for Institutional Review Boards (IRBs) | 17411 |
| 66 | Introduction to Public Health Research | 17637 |
| 67 | Public Health Research and Public Health Practice | 17638 |
| 68 | Informed Consent and Confidentiality in Public Health Research | 17639 |
| 69 | Ethical Issues in Public Health Research | 17640 |
| 70 | Introduction To Community-Engaged Research (CEnR) | 16994 |
| 71 | Introduction to Community-Based Participatory Research (CBPR) | 16995 |
| 72 | Human Subjects Considerations and Big Data Research | 19126 |
| 73 | Mobile Apps and Human Subjects Research | 19728 |
| 74 | Disaster and Conflict Research, Part 1: PI Responsibilities | 17384 |
| 75 | Disaster and Conflict Research, Part 2: Best Practices and Recommendations | 17385 |
| 76 | Ethical and Appropriate Uses of Administrative Data for Research and Evaluation | 19826 |
| 77 | Overview of the Clinical Trial Agreement (CTA) | 17356 |
Be aware that modules assigned to you may not all be posted in "Required Modules" section of your grade book.
Be sure to check the following sections for other modules you may need for CME credits:
- Optional Modules
- Elective Modules
- Supplemental Modules
Instructions and Requirements
You can only purchase 1 of the following 3 awards for CME credit.
Carefully select your option at point of purchase.
Earn 3 CME Credits:
- Complete 5 modules from the above list
- 70% passing score on each module
Earn 6 CME Credits:
- Complete 10 modules from the above list
- 70% passing score on each module
Earn 9 CME Credits (maximum award for this course):
- Complete 15 modules from the above list
- 70% passing score on each module
Need additional help?
Call 888-529-5929 during business hours or submit a request through our Support page with detailed information. Our team will follow up during business hours.