Many IRB approvals are delayed because of poorly prepared or incomplete submission documentation. A review may help you identify areas of the protocol that require clarification or additional ...

In this free webinar, understand the key benefits of master protocols. Attendees will identify the key challenges of master protocols and strategies to address them. The featured speakers will discuss ...

The following steps were used to achieve the objectives: Central Support: A central PSPO office was established with minimal required staffing for provision of support to clinicians for protocol ...

The Protocol Review and Monitoring Committee (PRMC) reviews all new cancer-related trials conducted at the institutions affiliated with the Case Comprehensive Cancer Center (Case CCC) and also ...

Institutional Biosafety Committee – recombinant DNA, materials of human or non-human primate origin, toxins, select agents, etc. Radiation Safety Committee – radioactive materials Institutional Review ...

Download the template(s) of your choice. The template documents open as Word files; save as a Word file to begin drafting your protocol. All instructions in the template are highlighted in blue.

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 ...

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 ...

If it’s possible a project will fall under the category of “research involving human subjects,” a great deal of preliminary planning will be required. It’s never too early to learn about the ethical ...

Developing and tweaking methods is a laborious and often unrewarded effort. With protocols.io, you can easily publish your protocols, making them citable and discoverable, getting the credit that you ...