The U.S. Food and Drug Administration (FDA) published the draft guidance “Protocol Deviations for Clinical Investigations of Drugs, ...

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).

If you are a participant (i.e., a student in PSY 120) and have questions, concerns, or issues related to your participation in research, please email psychstudies@purdue.edu. Once you have an approved ...

Protocols are created, edited, submitted, and managed via the Integrated Research Administration Portal (IRAP). The Animal Use Request/Registration (AUR) form is used for all types of protocol ...

Monthly Proposal and Revision Deadlines Protocols must be submitted and ready for IACUC ... You and anyone assisting with your research agree to be trained and appropriately qualified in those ...

IRB applications, including initial applications, amendments and continuing reviews, are accepted electronically via CyberIRB. CyberIRB is an online IRB submission system that researchers can access ...

As the curtain closed on 2024, FDA issued a new draft guidance to assist clinical trial sponsors, investigators, and institutional review ...

Flexible solar technology is a young but advancing industry. Scientists design unified testing protocol for flexible solar ...

In addition to original research, NEJM publishes reviews ... supplementary appendix, clinical trial protocol and statistical analysis plan (if applicable). Step 3: Submit your manuscript to ...

The IACUC is pleased to announce the launch of our new protocol software, eProtocol by Key Solutions as the electronic research administration system supporting animal research. Protocol development, ...

These collected resources can help when you're developing IRB protocols and related materials. If you have further questions after reviewing these materials, please contact our office. We also ...