Bryan Ennis, Chief Quality Officer & Founder at Sware, and Dan Tummillo, Pharmaceutical Compliance Consultant at 2RR, have an insightful conversation about how pharmaceutical companies can harness automation to streamline validation processes, mitigate risks, and boost operational efficiency.
In this session, Bryan and Dan discuss the key challenges pharma companies face with scattered data, slow validation processes, and reactive compliance efforts. They also explore how automating pharma validation can reduce human error, enable proactive reporting, provide real-time data access, and drive smarter decision-making—ultimately improving compliance and continuous quality improvement.
Pharma leaders: don’t miss this opportunity to learn how automation can transform your validation processes and keep you ahead of evolving regulatory demands.
