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What are the key ethical issues raised by this study?
What are the risks and benefits of study participation that should be listed in the consent form? Are these fair?
Should the IRB approve the study as it is currently designed?
What level of care should be provided for study participants?

These are all questions that an Institutional Review Board must answer when deciding whether to approve a proposal for a clinical research trial.

Join HUBS and The Johns Hopkins Berman Institute of Bioethics’ Dr. Dan O’Connor, who will be leading a mock IRB panel on a topic within International Research Ethics. See the conversations that determine whether a research study is ethical and the certain considerations necessary to have an ethical research project.

Thursday, April 11th 2013
7:00 pm in Charles Commons Ballroom C

Refreshments will be provided!

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