With psiXchange you now have a regulatory compliant workflow that automates the SUSAR distribution process so there are no manual steps associated with this activity.
You can manage your global reporting rules in a secure way, and send documents to any recipient, including sites, ECs, IRBs and authorities.
This means huge reductions in costs and efforts in every clinical trial along with much increased compliance oversight.
CROs and sponsors are already reporting significant return on investment when using psiXchange for this critical process.