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The Office Research Administration (ORA) is dedicated to assisting faculty and business administrators in the administration of sponsored awards. Training is...
Informed Consent You are likely to be presented with an informed consent form indicating approval by the IRB. This document is intended to provide you with...
Background and Educational Materials on Human Research CenterWatch: Background Information on Clinical Research NIH Clinical Center: Participate in Clinical...
Compliance Statement Yale University IRB is fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) , and...
Mission Yale strives to adhere to the highest ethical standards in the protection of human research participants and seeks to identify and implement means for...
The Yale University Radioactive Drug Research Program (Yale RDRC) program operates under federal regulation 21 CFR 361.1, which permits review and monitoring...
Yale University is committed to protecting the rights and welfare of individuals participating as subjects in its research. One way that the Yale HRPP assists...
Yale University is committed to ensuring that the research, consultation, and other activities of faculty and non–faculty employees are conducted in accordance...