psiXchange: Intelligent, Automated Clinical Trial Safety Reporting Software

Streamline your clinical trial safety reporting with psiXchange, your intelligent, automated solution. With psiXchange, you can bid farewell to manual burdens and welcome a streamlined process that automates the distribution, tracking, and acknowledgement of critical safety documents to key stakeholders such as Sites, Ethics Committees, Competent Authorities, and more, across 55 countries and beyond. Experience a significant reduction in time per submission (up to 90%) and operational costs (up to 80%) with psiXchange. Moreover, up to 95% site responsiveness rates will free your team from tedious manual tasks and allow them to focus on more important work. psiXchange is backed by a global team of pharmacovigilance professionals that deliver tangible results. One multinational biopharmaceutical company witnessed their site responsiveness rates soar from 41.2% to 95.2% within 24 months.

Download the infographic now to learn more about how psiXchange can empower your clinical trial safety reporting process.