What is an sIRB and Why Does my Study Need One?
Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.| Advarra
Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.| Advarra
Recent regulations and policies have many institutions establishing policies and processes for working with an external sIRB. Read more:| Advarra
Learn how Longboat is reimagining critical workflows across sites, sponsors, CROs, and patients.| Advarra
Internal IRB reviews are NOT free, contrary to popular belief. In this blog we outline practical steps for assessing and establishing IRB review cost| Advarra
Find out how the EU AI Act will likely impact clinical research software and systems, and what EU and non-EU entities should do to prepare for compliance.| Advarra
Assessing feasibility in clinical research is vital for success, enabling organizations to make informed decisions and ensure seamless execution and reporting of studies.| Advarra
This checklist offers a comprehensive framework for managing all necessary essential regulatory documents efficiently.| Advarra
A formal hazard communication or IBC SOP is critical to ensure clinical personnel understand the risks involved with genetically engineered investigational products.| Advarra
Explore key local considerations for developing single IRB policies, and learn how to navigate the challenges- including compliance, ethical standards, and institutional requirements.| Advarra
Ensure GCP compliance throughout your clinical research lifecycle with a comprehensive guide to GxP audits.| Advarra
