Recent regulations and policies have ushered in the era of mandated single IRB (sIRB) review. Many institutions must now establish policies and processes for working with an external sIRB.
Quantity of open studies isn’t always the best indicator of success. Be sure you ask these questions before taking on that next clinical trial.
In this Q&A, Dr. Luke Gelinas answers attendee questions from his webinar “Evaluating Payment to Participate in Research: Ethical and Regulatory Issues.”
Long activations is a familiar concept in the clinical trial landscape. How can your site improve your study activation timelines?
There are unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review and research informed consent.
There are many layers to a GCP audit. Explore the parts of an audit, what it accomplishes and how to effectively adhere to GCP.
Collaboration, Education and Fun in the Sun: Why You Should Attend the 2020 Spring Onsemble Conference
Our Spring 2020 Onsemble Conference is right around the corner, and nearly all of our sessions will qualify for continuing education units.
Site empowerment aims to improve the relationship between sites and their sponsors. Successful site-sponsor relationships all come down to establishing and upholding clear communication.