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.
This Clinical Trials Day, we want to celebrate the contribution made by your clinical research coordinators, and provide actionable ways to provide them with a fulfilling work environment.
Forte and ACRP partnered to conduct a survey analyzing the factors that contribute to technology competency and how sites, technology providers and clinical research professionals can work to improve these competencies across the industry.
Professional development and education are required in a vast array of industries, including clinical research. Continuing education units (CEUs) are a great way to have a record of your ongoing educational accomplishments.