The global pandemic has changed the way we think about research. Sponsors should consider how the “new normal” will impact sites and current studies as they plan to re-start research.
Learn how to find the right individual to manage your clinical research projects and improve the efficiency of your clinical trials.
Giving patients a choice in the way they are reimbursed for clinical trial participation can improve their overall trial experience. Learn how to incorporate participant preference in your research stipend plan.
Long activations is a familiar concept in the clinical trial landscape. How can your site improve your study activation timelines?
Empowering your staff and leaders within an organization starts with promoting a positive work environment. Learn about developing your team and building a successful career for yourself.
Creating a positive work environment is beneficial for everyone in the organization. Check out these 4 tips to enhance your organization’s culture.
Coordinating centers often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management System.
Good Clinical Practice benefits research in more ways than complying with the Food and Drug Administration. Learn more about why it’s important and how it helps achieve best practices of any clinical trial.
Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.