At NEXT, you’ll have an opportunity to hear provocative keynote presentations, engage in interactive, role-based sessions, and gain valuable, applicable knowledge for your business. Uncover best practices for effective design, planning, execution, management and reporting of clinical studies on a global scale, using the Medidata Clinical Cloud™.
Embarking upon a risk-based monitoring journey doesn’t have to be daunting. Our eBook, “The Ultimate Starter Kit for Risk-Based Monitoring (RBM),” can help you navigate each step, addressing and exploring core questions in light of recent revisions to regulatory guidance (ICH GCP E6).
Machine learning has been a buzz phrase in biopharma for some time now, even though some in the industry still struggle to define it. Many wonder whether the reality of artificial intelligence can live up to its hype and if it does have a serious role to play, whether regulators are ready to embrace its use.
The US Food and Drug Administration (FDA) recently published a guidance for industry on the use of electronic health record (EHR) data in FDA-regulated clinical investigations, with the goal of modernizing studies by using EHR data and including real-world data.
Advance your career among a passionate and diverse group of scientists, technologists, and designers, as we continue to transform clinical research in the hope for life-saving treatments. Join our collaborative, fast paced team where employees are given autonomy and encouraged to take risks. Are you ready for the challenge?