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 ...
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 ...
It may still be a few years off, but California State University, Northridge biology professor Rachel Mackelprang is part of ...
In some cases, applications can be based upon industry-accepted standards, as shown in Figure 10-27. For example, for devices that need to be able to connect to other devices to transfer data or to ...
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 ...
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