The IRB has released a new HRP-503 Protocol document, which was designed to make completing the document more efficient for researchers and reduce the number of revisions during the review process.

Follow the step-by-step instructions below to successfully prepare and submit a protocol to the IRB. Instructions below include information about single IRBs, student involvement in human subject ...

PHILADELPHIA--(BUSINESS WIRE)--TransCelerate BioPharma Inc. today announced the availability of an enhanced technology enabled Common Protocol Template (CPT). This update to the CPT is in alignment ...

Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

List of terms commonly used in clinical trial research. Glossary of Medical Terms in Lay Language Helpful list of medical terms described in lay language. Sample Study Startup Checklist Use this ...

Researchers may use the "Protocol Template" below to draft their protocol submission. Final versions of the protocols must be submitted via SPARCS. PROTOCOL Template All protocols are managed in the ...

When should you submit your IRB protocol submission? It is important to plan ahead and submit your IRB protocol submission ahead of time so it can be reviewed, processed, and approved by the CWRU IRB.

Animal protocol review is a lengthy process. We describe a repeatable approach using Generative Artificial Intelligence to improve the quality and speed of Institutional Animal Care and Use Committee ...

Researchers working with human subjects are required to submit their studies for review and approval by the Institutional Review Board (IRB). To streamline this process, our institution will be ...