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 prepare and submit a protocol to the IRB. Instructions below include information about single IRBs, student involvement in human subject ...

FDA, NIH & Industry Advance Templates for Clinical Trial Protocols The US Food and Drug Administration (FDA) and National Institutes of Health (NIH) on Tuesday released the final version of a common ...

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 ...

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.