Accelerating Clinical Trials Through Compliance Automation

Complion provides industry-leading solutions for eRegulatory and investigator site files. Their technology enables research sites, sponsors, and CROs to automate regulatory workflows, eliminating paper redundancies and manual processes. This allows faster study startup and accelerated enrollment. Complion's solutions include eReg for sites and eISF for sponsors and CROs. Key benefits include faster inspection readiness, decreased monitoring burden, and increased productivity.

Complion's technology has been implemented at over 22,000 sites across 50 countries. Having pioneered investigator regulatory tech over 10 years ago, Complion remains committed to advancing clinical research through continued innovation.