Drug Safety

Detection. Collection. Assessment. Monitoring.


Patient Support Programs play a crucial role in the identification of real world data that can impact a products development over time. Dosing or administration changes, and even new indications can occur as a result of adverse events or product quality complaints that our staff detect. Alio Health's Pharmacovigilance Program is a customizable solution that is compliant with all regulatory requirements. We work with clients to develop product specific SOPs for timely adverse event reporting, tracking and reconciliation. Our team undergoes extensive annual client-specific adverse event and product quality reporting training to ensure the specific requirements for timely reporting are met.

AE Tracking

Alio Health's AE Tracking System is a customizable fully integrated program for the collection and reporting of adverse events and product quality complaints. Program-required documents submitted by healthcare professionals are reviewed for adverse events and product quality complaints resulting in:

  • Error free DSS reconciliations
  • Annual client source data verification (SDV) audits with zero missed AEs
  • Excellent record of client PV audit and supplier quality assessment results