Medical device manufacturers must balance strict regulatory requirements, product traceability, and quality system expectations while managing frequent change across products and processes. This session demonstrates how Epicor Kinetic functions as a compliance focused foundation and how it works in combination with other Epicor software solutions and partner technologies to support efficient, controlled workflows. Attendees will see how core Kinetic capabilities support design history, production records, and change management, while complementary tools address validation and operational complexity. The session also highlights how Epicor Test ReCoder can be used to automate aspects of software validation testing as part of broader compliance and upgrade readiness strategies.

• Understand Kinetic’s role as a regulated software solution
• See how Epicor solutions extend workflows across quality and operations.
• Learn how Test ReCoder supports automated software validation testing.

This session provides a practical view of how coordinated Epicor solutions help medical device manufacturers manage compliance with confidence.