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.
Virtual trials have grown in popularity and usage over the last decade. Explore what that means for traditional sites and their future in the clinical research landscape.
Implementing and integrating a CTMS can be beneficial for your organization. Streamline your research operations with these 4 integrations.
The NCI sets high standards for protocol activation timelines. While the expectation for protocols to be activated in 8-12 weeks, is it achievable? What can be done to improve study start up time?