While maintaining software compliance is crucial for Life Sciences teams, mounting pressures from the Business, a rapidly evolving IT landscape, and new guidance from the FDA are causing many in the industry to re-evaluate the way they manage computer systems validation. In response, the adoption of Digital Validation is becoming increasingly prevalent as more and more teams are recognizing the need to shed traditional document-centric frameworks.

Join this session to learn how Digital Validation, supported by Vera and qTest, can enable your organization to achieve streamlined, modern software compliance.

Jason Tepfenhardt
VP of HLS and SW Quality & Compliance, Tricentis

Henry Farris
Product Management – Vera, Tricentis