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 ...

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 ...

Via well-designed AI tools and workflows, trial sponsors are aiming to unify cross-functional data ecosystems to enable a ...

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 ...

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.

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 ...

An Investigational New Drug (IND) is a drug or biological drug that has not been approved for general use by the FDA. It is used in a clinical trial to investigate its safety and efficacy. The term ...