In most cases, no protocol, consent process ... must report such incidents to the Sponsor and/or the FDA as well as the IRB. See the section on Reporting Research-Related Problems for definitions and ...

Repeats of classic earlier research in classroom settings is usually considered ... Will subjects be deceived intentionally as part of the protocol? Occasionally, deception of subjects is essential to ...

Protocols are created, edited, submitted, and managed via the Integrated Research Administration Portal (IRAP ... and details included in the appropriate sections of the Species form(s). Be sure to ...

By submitting a request, you are affirming that the study posted on Sona is based on a research protocol that has been approved by ... the following information must be included in the designated ...

Research protocols that have not been fully approved by the Drexel ... Policies and Procedures are to be included in documentation made available to all sections of PSY 101, 111, and 112. Psychology ...

Use of vertebrate animals in research, teaching or testing at Purdue University or its affiliated sites requires approval of a protocol by the Institutional Animal Care and Use Committee (IACUC).

The trial number must be clearly indicated in the abstract and methods section of the manuscript ... should be pre-specified in the study protocol. Preliminary analyses of ongoing clinical ...

Your Animal Use Protocol has been completed and submitted in the eProtocol software. As a federally funded institution, the University of Nevada, Reno will hold all research conducted at the ...

and the Alicante Institute for Health and Biomedical Research (ISABIAL), have developed a cellular fractionation protocol.

Studies that involve prospective tissue research also require review by the PRMC. The PRMC plays a critical role in protocol review and monitoring to ensure that clinical trials are scientifically ...