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.

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Submissions from 2011

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Sponsor-investigator responsibilities IND, Christy Auston and Jeanne Velders

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Historical timeline, Sarah Fowler-Dixon

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Research with human subjects, Sarah Fowler-Dixon

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Successful human subject research, Sarah Fowler-Dixon and Mickey Clarke

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Consent, Jonathan Green

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IRB review of device studies, Jonathan Green

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Challenges with consent, Jonathan Green and Jeanne Velders

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Study start-up for industry initiated studies:Site responsibilities to seriously consider feasibility for the study at WU, Phyllis Klein

Submissions from 2010

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Researching research seminar: ethical framework in research involving human participants, Martha J. Jones

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Navigating the IRB, Martha J. Jones

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IRB basics, Jeanne Velders

Submissions from 2008

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Education of researchers, Sarah Fowler-Dixon

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IRB consortia as an approach to facilitating effective and efficient reviews, Sarah Fowler-Dixon

Submissions from 2007

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Certificate of confidentiality guideline, Sarah Fowler-Dixon

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HRPO internet research guideline, Sarah Fowler-Dixon

Submissions from 2006

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International Committee on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Sarah Fowler-Dixon

Submissions from 2005

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What are the ethics?, Sarah Fowler-Dixon

Submissions from 2004

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An education program for busy researchers, Sarah Fowler-Dixon

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Conducting your study, Sarah Fowler-Dixon

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Inconsistency of IRB review: A research project, Sarah Fowler-Dixon

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Vulnerable populations, Sarah Fowler-Dixon

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Ethical issues in human subjects research, Martha Jones and Sarah Fowler-Dixon

Submissions from 2003

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Defining clinical trials: Education in human research protection, Sarah Fowler-Dixon

Submissions from 2002

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Ethical issues confronting clinical research: How did we get here?, Sarah Fowler-Dixon