In carrying out its mission, the Human Research Protection Office offers a wide variety of standalone workshops and presentations. Presentations, listed by title, are available below. Items contained in this section are also searchable using key words such as: consent, devices, diversity, ethics, history, IRB, legal issues, study process, technology, and vulnerable participants or subjects.
Presentations from 2024
Requesting to Rely NCI & External IRBs, Carissa Minder
Presentations from 2022
Ethical Discussion of the Need for IRB Approval, Sarah Fowler-Dixon
Presentations from 2021
Showing impact through data collection, Niki Bridges
Presentations from 2011
Sponsor-investigator responsibilities IND, Christy Auston and Jeanne Velders
Historical timeline, Sarah Fowler-Dixon
Research with human subjects, Sarah Fowler-Dixon
Successful human subject research, Sarah Fowler-Dixon and Mickey Clarke
Consent, Jonathan Green
IRB review of device studies, Jonathan Green
Challenges with consent, Jonathan Green and Jeanne Velders
Study start-up for industry initiated studies:Site responsibilities to seriously consider feasibility for the study at WU, Phyllis Klein
Presentations from 2010
Navigating the IRB, Martha F. Jones
Researching research seminar: ethical framework in research involving human participants, Martha F. Jones
IRB basics, Jeanne Velders
Presentations from 2008
Education of researchers, Sarah Fowler-Dixon
IRB consortia as an approach to facilitating effective and efficient reviews, Sarah Fowler-Dixon
Presentations from 2007
Certificate of confidentiality guideline, Sarah Fowler-Dixon
HRPO internet research guideline, Sarah Fowler-Dixon
Presentations from 2006
International Committee on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Sarah Fowler-Dixon
Presentations from 2005
What are the ethics?, Sarah Fowler-Dixon
Presentations from 2004
An education program for busy researchers, Sarah Fowler-Dixon
Conducting your study, Sarah Fowler-Dixon
Inconsistency of IRB review: A research project, Sarah Fowler-Dixon
Vulnerable populations, Sarah Fowler-Dixon
Ethical issues in human subjects research, Martha Jones and Sarah Fowler-Dixon
Presentations from 2003
Defining clinical trials: Education in human research protection, Sarah Fowler-Dixon
Presentations from 2002
Ethical issues confronting clinical research: How did we get here?, Sarah Fowler-Dixon
