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 ...

In order to address the specific details and regulatory requirements present in a retrospective medical chart review, the UB IRB recently created a new Protocol template: the HRP-503R. In order to ...

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 ...

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.

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

The Principal Investigator (PI) is responsible for reviewing this policy and complying with its requirements. Specifically, the PI will: You may use the protocol template to record your information ...

Clinical trials are critical for bringing new treatments and therapies to market, but they are also time-consuming, expensive, and complex. Protocol development is a crucial component of the clinical ...

Each School and Faculty have developed a suite of study document templates based on key ethical issues. Applicants are encouraged to use the templates when developing their research ethics application ...