Thank You Thank you for registering for our event! We look forward to seeing you. Featured Content Blog “Single IRB” vs “Central IRB” – What’s the Difference? With the rise of single IRB (sIRB) mandates, understanding the nuances between sIRB and central IRB (cIRB) is crucial for multisite studies. Read More… Blog Beginner’s Guide to Clinical Trial Management Systems From the largest research centers to the smallest, sites now recognize that a clinical trial management system (CTMS) can be configured to their needs and can bring powerful efficiencies insights, and compliance to their day-to-day operations. Read More… Blog Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents Efficient document systems like eTMF and eISF enhance compliance and streamline document management, helping sites and sponsors ensure secure, organized trial records. Read More… Blog Improving Study Activation Time for Gene Therapy Research This blog explores how research sites are focusing on their institutional biosafety committee (IBC) programs as part of overall study activation time. Read More… Visit the Resource Library Ready to Advance Your Clinical Research Capabilities? Contact Us
